Ignite Creation Date:
2024-05-06 @ 7:50 PM
Last Modification Date:
2024-10-26 @ 3:15 PM
Study NCT ID:
NCT06155578
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-12-04
First Post:
2023-11-24
Brief Title:
Safety and Efficacy of Topical Sodium Metabisulfite for the Treatment of Calcinosis in Patients With Systemic Sclerosis
Sponsor:
Pontificia Universidad Catolica de Chile
Organization:
Pontificia Universidad Catolica de Chile
Study Overview
Official Title:
Randomized Placebo-controlled Trial of the Safety and Efficacy of Topical Sodium Metabisulfite for the Treatment of Calcinosis in Patients With Systemic Sclerosis
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
Cal-23
Brief Summary:
This prospective placebo-controlled trial will enroll 20 patients with SSc and at least one calcinotic lesion of the hands that is palpable on physical examination and measurable on hand radiographs Each subject will undergo a screening evaluation 1 month before treatment with the study drug is initiated Each subject will be instructed to blindly self-apply either topical 25 sodium metabisulfite or placebo cream twice daily In-person follow-up evaluations will be performed after 4-months with monthly telehealth follow-up visits to ensure adherence and arrange study drug refill deliveries
Detailed Description:
1 Background
Calcinosis cutis is the deposition of calcium in the skin and subcutaneous tissues It is a common and debilitating manifestation of systemic sclerosis SSc affecting 1 in 4 of these patients over the course of their disease Calcinosis in SSc occurs most frequently in the hands particularly the fingers and within the fingers most commonly in the thumbs or index of the dominant hand Calcinosis in SSc can cause pain soft tissue swelling around the calcium deposits ulcers with superimposed infection or deformities leading to significant impact on quality of life
Treatment for calcinosis cutis is often difficult and unsuccessful and remains an unmet need in patients with SSc Evidence mainly comes from small retrospective studies case series and case reports since no large prospective randomized controlled trials have been conducted The response to various agents such as topical or oral aluminum hydroxide topical or intralesional sodium thiosulfate intralesional corticosteroids calcium-channel blockers minocycline bisphosphonates and surgical excision has remained largely unsatisfactory
Topical intralesional and intravenous IV sodium thiosulfate have been studied as treatments for disorders of cutaneous calcium deposition The mechanism of sodium thiosulfate in the treatment of calcium-related disorders is thought to be multifactorial It is believed to act by transforming calcium into calcium thiosulfate salts thus increasing calcium solubility In addition it may increase the production of hydrogen sulfide which has vasodilatory antioxidant and anti-inflammatory properties and may cause direct inhibition of vascular calcifications
Sodium metabisulfite SM is an inorganic compound used as a disinfectant antioxidant and preserving agent that when reacting with oxygen becomes sodium sulfate a metabolite of sodium thiosulfate that has a similar ability to inhibit calcium oxalate agglomeration and calcium stone formation In 2016 topical 25 SM was used for the first time in four patients with dystrophic calcinosis cutis one with SSc two with dermatomyositis and one with radio-dermatitis after breast cancer showing significant decrease in size erythema and pain The authors hypothesized that topical SM may dissolve calcium deposits and promote local vasodilation and wound healing Since then topical sodium metabisulfite use has been reported as an inexpensive safe and promising new agent for the treatment of calcinosis cutis
On behalf of the Scleroderma Clinical Trial Consortium SCTC Calcinosis Working Group we developed and validated a novel radiographic scoring system to assess the severity of calcinosis affecting the hands of patients with SSc that accounts for area coverage density and anatomic location This scoring system is feasible and was found to have excellent intra- and inter-rater reliability with intra-class correlation coefficients ICC of 93 89-97 and 89 86-92 respectively We confirmed the excellent inter-rater reliability of our radiographic calcinosis scoring system and demonstrated its usefulness to detect change over time in a recent study of 39 patients and a validation cohort of 19 patientsCalcinosis in SSc usually progresses over time In this same study 80 of patients had worsening or unchanged calcinosis without treatment at 1 year follow-up as measured by this radiologic scoring system
Given that calcinosis is a frequent debilitating and progressive complication of SSc with no effective therapies a clinical trial using novel outcome measures testing the safety and efficacy of a potential treatment of calcinosis is warranted
2 PrimarySecondary objectives
Our main objective is to conduct a study with the following primary and secondary endpoints
Primary endpoints
To assess the safety and tolerability of using topical 25 SM applied twice daily in SSc patients with calcinosis affecting the hands
To assess the efficacy of topical 25 SM versus placebo in stabilizing the calcinosis burden or reducing the radiographic progression of calcinosis over four months
Secondary endpoints
To assess the effect of topical 25 SM on the change in the Mawdsley Calcinosis Questionnaire and patient and physician assessment of calcinosis severity over four months
To assess the effect of topical 25 SM on the change in size of calcinosis on ultrasound
To assess the presence of markers of vascular damage by tape stripping in SSc patients with calcinosis
3 Hypothesis
We hypothesize that topical SM may be beneficial in the treatment of calcinosis in patients with SSc stabilizing the burden of calcinosis as measured by the SCTC radiologic scoring system
4 Study design
This prospective placebo-controlled trial will enroll 20 patients with SSc and at least one calcinotic lesion of the hands that is palpable on physical examination and measurable on hand radiographs Each subject will undergo a screening evaluation 1 month before treatment with the study drug is initiated Each subject will be instructed to blindly self-apply either topical 25 SM or placebo cream twice daily Follow-up in-person evaluations will be performed a 4-month period with monthly telehealth follow-up visits to ensure adherence and provide study drug
5 Study population
The population for this study will consist of adult SSc patients with evidence of at least one calcinotic lesion of the hands that is palpable on physical examination and measurable on hand radiographs Inclusion and exclusion criteria have been entered elsewhere
6 Description of the treatment
Each subject will be randomized and instructed to blindly self-apply either SM prepared in pediatric cold cream water in oil emulsion at a concentration of 25 or placebo topically twice daily which will be continued as tolerated Vinyl gloves will be supplied to each patient to improve topical absorption Patients will participate in a learning session with examples and instructions on how to use the cream Detailed instructions will be provided to patients for their reference during treatment
7 Description of Assessments
Medical history including SSc Significant past or present illnesses current prescription or nonprescription medications including vitamins and herbal products and history of allergies or idiosyncratic responses to drugs will be noted at the time of enrolment Demographic and clinical data including age gender race smoking status disease duration defined from onset of RP and from first non-RP symptom SSc skin subtype internal organ involvement and auto-antibodies including SSc-specific and anti-phospholipid antibodies will be recorded
Physical examination A complete physical examination will be conducted by a physician at screening baseline and at end of study
Vital Signs Systolic and diastolic blood pressure heart rate and temperature C will be measured after sitting for 5 minutes at screening baseline and 4 months Vital signs should also be assessed in the case of abnormal clinical signs and symptoms
Laboratory tests Blood and urine samples for the measurement and evaluation of routine blood laboratory test CBC CMP and pregnancy urine test for fertile women will be collected at screening and at the end of the study
Tape stripping Skin samples will be obtained using the tape stripping technique utilizing five standard D-Squame sampling discs Cuderm Dallas USA at the same site on the hands before the initiation of topical treatment with SM or a placebo and at the conclusion
Radiological examination of calcinosis Descripcion has been entered elsewhere
Ultrasonography US Descripcion has been entered elsewhere
Mawdsley Calcinosis Questionnaire MCQ Descripcion has been entered elsewhere
Patient and Physician global assessments Descripcion has been entered elsewhere
8 Safety monitoring and reporting Safety During the study the primary assessment of safety will be the development of adverse events
Adverse Event AE An AE is any untoward medical experience occurring to a subject during a clinical trial whether it is related to the study drug An AE may include an intercurrent illness injury or any other concomitant impairment of the subjects health as well as abnormal laboratory findings if deemed to have clinical significance AEs may also include worsening of an existing symptom or condition or post-treatment events that occur because of protocol-mandated procedures
Severe Adverse Event SAE A SAE is an AE occurring at any dose that results in any of the following outcomes
Death
A life-threatening AE
Inpatient hospitalization or prolongation of existing hospitalization
A persistent or significant disability incapacity
A congenital anomaly birth defect
In addition important medical events that may not result in death be life-threatening or require hospitalization may be considered serious when based upon appropriate medical judgment they may jeopardize the subject and require medical surgical intervention to prevent one of the outcomes listed above
9 Statistical Considerations
Statistical analysis
Descriptive statistics and frequency distributions of all variables of interest will be reported as proportions for categorical variables and as mean standard deviation or median range for continuous variables Baseline to 4-month differences and 95 confidence intervals will be calculated for scored outcomes x-ray score physicians global assessment by VAS and quality of life measurements For the primary efficacy endpoint mean change and standard deviation in calcinosis burden assessed by radiograph from baseline to 4-month visit we will use Students t-test The mean rate of change of calcinosis in radiograph will be calculated with the following formula Year 1 XR score - Baseline XR scoretime XR score is defined as sum of scores for 22 weighted areas affecting each hand area coverage 0-100 X density 1-3 X weight for each area19
Sample size calculation
We are planning a study of a continuous response variable from independent control and experimental subjects with 1 controls per experimental subject In a previous study the response within each subject group was normally distributed with standard deviation 32 If the true difference in the experimental and control means is 42 we will need to study 10 experimental subjects and 10 control subjects to be able to reject the null hypothesis that the population means of the experimental and control groups are equal with probability power 08 The Type I error probability associated with this test of this null hypothesis is 005
10 Risks of Treatment The main risks of the treatment are the same as those secondary to the use of any other cream or topical treatment participants may experience burning pain or allergies in the treatment area In case of any of these adverse effects the participant will be evaluated by a Dermatologist member of our team
However in a 2022 review in which the best scientific evidence of all published works that included the use of sodium metabisulfite cream for the treatment of skin calcifications in autoimmune patients was analyzed out of a total of 7 patients none of them presented any adverse effect with the application of said cream so with the current evidence to date the probability of presenting any adverse effect from the use of this topical treatment is very low that is less than 01 or less than 1 person in every 1000 people who use this cream
Calcinosis cutis is the deposition of calcium in the skin and subcutaneous tissues It is a common and debilitating manifestation of systemic sclerosis SSc affecting 1 in 4 of these patients over the course of their disease Calcinosis in SSc occurs most frequently in the hands particularly the fingers and within the fingers most commonly in the thumbs or index of the dominant hand Calcinosis in SSc can cause pain soft tissue swelling around the calcium deposits ulcers with superimposed infection or deformities leading to significant impact on quality of life
Treatment for calcinosis cutis is often difficult and unsuccessful and remains an unmet need in patients with SSc Evidence mainly comes from small retrospective studies case series and case reports since no large prospective randomized controlled trials have been conducted The response to various agents such as topical or oral aluminum hydroxide topical or intralesional sodium thiosulfate intralesional corticosteroids calcium-channel blockers minocycline bisphosphonates and surgical excision has remained largely unsatisfactory
Topical intralesional and intravenous IV sodium thiosulfate have been studied as treatments for disorders of cutaneous calcium deposition The mechanism of sodium thiosulfate in the treatment of calcium-related disorders is thought to be multifactorial It is believed to act by transforming calcium into calcium thiosulfate salts thus increasing calcium solubility In addition it may increase the production of hydrogen sulfide which has vasodilatory antioxidant and anti-inflammatory properties and may cause direct inhibition of vascular calcifications
Sodium metabisulfite SM is an inorganic compound used as a disinfectant antioxidant and preserving agent that when reacting with oxygen becomes sodium sulfate a metabolite of sodium thiosulfate that has a similar ability to inhibit calcium oxalate agglomeration and calcium stone formation In 2016 topical 25 SM was used for the first time in four patients with dystrophic calcinosis cutis one with SSc two with dermatomyositis and one with radio-dermatitis after breast cancer showing significant decrease in size erythema and pain The authors hypothesized that topical SM may dissolve calcium deposits and promote local vasodilation and wound healing Since then topical sodium metabisulfite use has been reported as an inexpensive safe and promising new agent for the treatment of calcinosis cutis
On behalf of the Scleroderma Clinical Trial Consortium SCTC Calcinosis Working Group we developed and validated a novel radiographic scoring system to assess the severity of calcinosis affecting the hands of patients with SSc that accounts for area coverage density and anatomic location This scoring system is feasible and was found to have excellent intra- and inter-rater reliability with intra-class correlation coefficients ICC of 93 89-97 and 89 86-92 respectively We confirmed the excellent inter-rater reliability of our radiographic calcinosis scoring system and demonstrated its usefulness to detect change over time in a recent study of 39 patients and a validation cohort of 19 patientsCalcinosis in SSc usually progresses over time In this same study 80 of patients had worsening or unchanged calcinosis without treatment at 1 year follow-up as measured by this radiologic scoring system
Given that calcinosis is a frequent debilitating and progressive complication of SSc with no effective therapies a clinical trial using novel outcome measures testing the safety and efficacy of a potential treatment of calcinosis is warranted
2 PrimarySecondary objectives
Our main objective is to conduct a study with the following primary and secondary endpoints
Primary endpoints
To assess the safety and tolerability of using topical 25 SM applied twice daily in SSc patients with calcinosis affecting the hands
To assess the efficacy of topical 25 SM versus placebo in stabilizing the calcinosis burden or reducing the radiographic progression of calcinosis over four months
Secondary endpoints
To assess the effect of topical 25 SM on the change in the Mawdsley Calcinosis Questionnaire and patient and physician assessment of calcinosis severity over four months
To assess the effect of topical 25 SM on the change in size of calcinosis on ultrasound
To assess the presence of markers of vascular damage by tape stripping in SSc patients with calcinosis
3 Hypothesis
We hypothesize that topical SM may be beneficial in the treatment of calcinosis in patients with SSc stabilizing the burden of calcinosis as measured by the SCTC radiologic scoring system
4 Study design
This prospective placebo-controlled trial will enroll 20 patients with SSc and at least one calcinotic lesion of the hands that is palpable on physical examination and measurable on hand radiographs Each subject will undergo a screening evaluation 1 month before treatment with the study drug is initiated Each subject will be instructed to blindly self-apply either topical 25 SM or placebo cream twice daily Follow-up in-person evaluations will be performed a 4-month period with monthly telehealth follow-up visits to ensure adherence and provide study drug
5 Study population
The population for this study will consist of adult SSc patients with evidence of at least one calcinotic lesion of the hands that is palpable on physical examination and measurable on hand radiographs Inclusion and exclusion criteria have been entered elsewhere
6 Description of the treatment
Each subject will be randomized and instructed to blindly self-apply either SM prepared in pediatric cold cream water in oil emulsion at a concentration of 25 or placebo topically twice daily which will be continued as tolerated Vinyl gloves will be supplied to each patient to improve topical absorption Patients will participate in a learning session with examples and instructions on how to use the cream Detailed instructions will be provided to patients for their reference during treatment
7 Description of Assessments
Medical history including SSc Significant past or present illnesses current prescription or nonprescription medications including vitamins and herbal products and history of allergies or idiosyncratic responses to drugs will be noted at the time of enrolment Demographic and clinical data including age gender race smoking status disease duration defined from onset of RP and from first non-RP symptom SSc skin subtype internal organ involvement and auto-antibodies including SSc-specific and anti-phospholipid antibodies will be recorded
Physical examination A complete physical examination will be conducted by a physician at screening baseline and at end of study
Vital Signs Systolic and diastolic blood pressure heart rate and temperature C will be measured after sitting for 5 minutes at screening baseline and 4 months Vital signs should also be assessed in the case of abnormal clinical signs and symptoms
Laboratory tests Blood and urine samples for the measurement and evaluation of routine blood laboratory test CBC CMP and pregnancy urine test for fertile women will be collected at screening and at the end of the study
Tape stripping Skin samples will be obtained using the tape stripping technique utilizing five standard D-Squame sampling discs Cuderm Dallas USA at the same site on the hands before the initiation of topical treatment with SM or a placebo and at the conclusion
Radiological examination of calcinosis Descripcion has been entered elsewhere
Ultrasonography US Descripcion has been entered elsewhere
Mawdsley Calcinosis Questionnaire MCQ Descripcion has been entered elsewhere
Patient and Physician global assessments Descripcion has been entered elsewhere
8 Safety monitoring and reporting Safety During the study the primary assessment of safety will be the development of adverse events
Adverse Event AE An AE is any untoward medical experience occurring to a subject during a clinical trial whether it is related to the study drug An AE may include an intercurrent illness injury or any other concomitant impairment of the subjects health as well as abnormal laboratory findings if deemed to have clinical significance AEs may also include worsening of an existing symptom or condition or post-treatment events that occur because of protocol-mandated procedures
Severe Adverse Event SAE A SAE is an AE occurring at any dose that results in any of the following outcomes
Death
A life-threatening AE
Inpatient hospitalization or prolongation of existing hospitalization
A persistent or significant disability incapacity
A congenital anomaly birth defect
In addition important medical events that may not result in death be life-threatening or require hospitalization may be considered serious when based upon appropriate medical judgment they may jeopardize the subject and require medical surgical intervention to prevent one of the outcomes listed above
9 Statistical Considerations
Statistical analysis
Descriptive statistics and frequency distributions of all variables of interest will be reported as proportions for categorical variables and as mean standard deviation or median range for continuous variables Baseline to 4-month differences and 95 confidence intervals will be calculated for scored outcomes x-ray score physicians global assessment by VAS and quality of life measurements For the primary efficacy endpoint mean change and standard deviation in calcinosis burden assessed by radiograph from baseline to 4-month visit we will use Students t-test The mean rate of change of calcinosis in radiograph will be calculated with the following formula Year 1 XR score - Baseline XR scoretime XR score is defined as sum of scores for 22 weighted areas affecting each hand area coverage 0-100 X density 1-3 X weight for each area19
Sample size calculation
We are planning a study of a continuous response variable from independent control and experimental subjects with 1 controls per experimental subject In a previous study the response within each subject group was normally distributed with standard deviation 32 If the true difference in the experimental and control means is 42 we will need to study 10 experimental subjects and 10 control subjects to be able to reject the null hypothesis that the population means of the experimental and control groups are equal with probability power 08 The Type I error probability associated with this test of this null hypothesis is 005
10 Risks of Treatment The main risks of the treatment are the same as those secondary to the use of any other cream or topical treatment participants may experience burning pain or allergies in the treatment area In case of any of these adverse effects the participant will be evaluated by a Dermatologist member of our team
However in a 2022 review in which the best scientific evidence of all published works that included the use of sodium metabisulfite cream for the treatment of skin calcifications in autoimmune patients was analyzed out of a total of 7 patients none of them presented any adverse effect with the application of said cream so with the current evidence to date the probability of presenting any adverse effect from the use of this topical treatment is very low that is less than 01 or less than 1 person in every 1000 people who use this cream
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None