Ignite Creation Date:
2024-05-06 @ 3:38 PM
Last Modification Date:
2024-10-26 @ 1:54 PM
Study NCT ID:
NCT04709419
Status:
TERMINATED
Last Update Posted:
2024-01-11
First Post:
2021-01-11
Brief Title:
Celliant Socks to Increase Tissue Oxygenation and Complete Wound Closure in Diabetic Foot Wounds
Sponsor:
University of Texas Southwestern Medical Center
Organization:
University of Texas Southwestern Medical Center
Study Overview
Official Title:
Study to Evaluate Celliant Diabetic Medical Socks to Increase Tissue Oxygenation and Incidence of Complete Wound Closure in Diabetic Foot Wounds
Status:
TERMINATED
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
unable to enroll
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is a prospective multicenter double-blind 11 randomized clinical trial The purpose of this study is to demonstrate that the use of Celliant Socks increases tissue oxygenation via oxygen saturation StO2 and incidence of wound closure in subjects with diabetic foot ulcers This study will use hyperspectral imaging and wound assessment to measure these outcomes The study will enroll 254 evaluable subjects total 127 per arm to meet the Primary Endpoint Enrollment may continue up to twenty-five hundred 2500 evaluable subjects total to meet the Key Secondary Endpoint of complete wound closure
Detailed Description:
Screening and Enrollment
Patients who present to the investigators institution through clinic admission direct transfer from another facility or through the emergency room may be recruited to participate in the study No direct marketing for subject recruitment will be done
Patients approached for study participation will be at least 22 years of age at the time of consent will undergo wound assessment and meet all eligibility requirements Those meeting eligibility criteria for the study will have the study explained to them by the Investigator An Informed Consent Form will be provided to sign according to Section 11 prior to undergoing any study procedures Patients will be encouraged to ask questions of the investigators It will be made clear to the patient that not participating in the study will in no way influence the treatment plan or the relationship with the physician
Wound Selection
Only one wound per subject will be included in the study Subjects with multiple wounds will have each wound measured for volume The wound with the largest volume meeting all eligibility requirements will be chosen for inclusion in the study The etiology of the chosen wound and if it is a new or recurring will be documented
Randomization and Blinding Procedure
Prior to study initiation Active and Control samples will be prepared in sealed and labeled as A or B also randomization envelopes will be provided to the research staff and used to obtain randomization assignment Within each randomization envelope there is an assignment of A or B After run-in evaluation the subjects wound will be debrided and dressed with SOC At the end of the procedure subjects who continue to meet all inclusion and no exclusion criteria will be randomized in a 11 ratio to be treated with either Control or Celliant therapies stratified by wound size greater than size of 4 cm2 and study center Study staff will use the randomization number labels and sock assignment of socks A or B contained in the envelope The number will become the subject ID The research staff will note the randomization number and the treatment assignment letter A or B on the CRF The key indicating therapy assignments Active or Control will only be available to staff not directly involved in the study until after the subject has completed study activities
Visit Schedule
Study procedures for each phase of study are outlined below In a later section details on each study procedure are described including equipment designation
Screening
1 Explain purpose and nature of the study and obtain signature on the informed consent document
2 Screen the subject against protocol inclusion and exclusion criteria including all pertinent tests
1 ABI andtoe pressure
2 Ulcer History measurement and classification
3 Urine Pregnancy test if indicated
Baseline may be done as same day as screening procedures
1 Obtain general medical history and demographic information and social history
2 Complete a physical examination body weight height and vital signs including measurement of resting heart rate respiratory rate and blood pressure while seated
3 Select the target ulcer
4 Obtain complete history pertinent to DFU disease including duration of the target ulcer previous and current treatment
5 Perform debridement if indicated Debridement is to be performed using curette scissors scalpel or forceps
6 Perform standardized photography and measurement of the study wound eKare or available camera with ruler Assess the post-debridement ulcer area cm2 perimeter cm and greatest depth cm using the inSight device eKare Fairfax VA These values are the baseline measurements for assessing accelerated wound closure at the two-week run-in visit
7 Perform baseline SPP note - this procedure does not need to be performed at baseline visit and can be performed at any visit through Run-In week 2Therapy initiation visit
8 Perform baseline tcpO2 note - this procedure does not need to be performed at baseline visit and can be performed at any visit through Run-In week 2Therapy initiation visit
9 Perform baseline hyperspectral imaging assessment on the dorsal and plantar aspects of the foot
10 Perform neuropathy and pain assessment
11 Obtain blood for hematology blood chemistry etc that were not covered in inclusionexclusion studies
12 Subjects who do not meet eligibility and fail to qualify to enter the Run-in will be deemed Screen failures and discharged noting the reasons for disqualification
13 Collect all relevant concomitant medication antibiotics antifungals and other anti-infective therapies
14 Wounds will be dressed SOC and offloaded per physician discretion
15 Subjects who qualify to enter the run-in will be instructed to refrain from using excluded medications and return to the office for Run-in Visit 2 within 7 1 days
Run-In ProceduresTherapy Initiation
Week 1 Run-in
1 Assess target ulcer
2 Perform debridement if indicated Debridement is to be performed using a curette scissors scalpel or forceps
3 Perform standardized photography of the study wound
4 Assess the post-debridement ulcer area cm2 perimeter cm and greatest depth cm using the inSight device
5 If wound size ulcer area increasesdecreases by 30 or more patient will be deemed a screen failure and removed from the study
6 If wound size ulcer area decreases by less than 30 patient wound will be treated with standard of care and return for run-in Week 2 Run-In within 7 1 days
7 Perform hyperspectral imaging assessment on the dorsal and plantar aspects of the foot
8 Perform pain assessment
9 Collect all relevant concomitant medication antibiotics antifungals and other anti-infective therapies
10 Wounds will be dressed SOC and offloaded per physician discretion
Week 2 Run-inTherapy Initiation
1 Assess target ulcer
2 Perform debridement if indicated Debridement is to be performed using curette scissors scalpel or forceps
3 Perform standardized photography of the study wound
4 Assess the post-debridement ulcer area cm2 perimeter cm and greatest depth cm using the inSight device
5 If wound size ulcer area increasesdecreases by 30 or more patient will be deemed a screen failure and removed from the study
6 If wound size ulcer area increasesdecreases by less than 30 patient wound will enter the study and randomized to either the Celliant Active or Control treatment arm
7 Perform hyperspectral imaging of the dorsal and plantar aspects of the foot
8 Perform pain assessment
9 Collect all relevant concomitant medication
10 Wound will be dressed with SOC and either Celliant Active or Control Sock applied
11 Wound will be offloaded
12 Provide subject with any additional medical socks needed until the next visit Instruct the subject to change the socks if they become wet soiled or bloody and under any conditions dictated by PI instructions
TherapyTreatment Phase
Study Visit 1-11
1 Document study compliance information from the subject
1 Amount of time the sock was worn throughout the week
2 Was it worn during the daynight
3 Whenwhy the sock was changed
4 Has the sock been on in the 3 hours leading up to the appointment
2 Remove sock and dressing and immediately perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed
3 Assess target ulcer if wound has closed document as such perform steps 7 and 8 and skip to Study Visit - Wound Closed
4 Debridement is to be performed if indicated using curette scissors scalpel or forceps If debridement is necessary at weekly visits all therapy must be removed and replaced post-debridement
5 Perform standardized photography of the study wound
6 Assess the ulcer area cm2 perimeter cm and greatest depth cm using the inSight device - if the wound is deemed closed by the physician skip to EOS visit
7 Perform SPP and tcPO2 measurements at Visit 4 maybe be taken instead at visit 5 or 6 if subject has not been wearing their treatment sock leading up to the visit or misses this visit
8 Collect all relevant concomitant medication
9 Perform pain assessment
10 Redress the wound with standard of care if wound is still active and apply Celliant Active or Control Sock and apply offloading if indicated
11 Wound will be offloaded
12 Provide subject with any additional medical socks needed until the next visit Instruct the subject to change the socks if they become wet soiled or bloody and under any conditions dictated by PI instructions Instruct the subject that they must wear the sock at all times and that including the 3 hours leading up to the next study visit
Study Visit - Wound Closed
1 The study wound is defined as closed when there is complete skin re-epithelialization without drainage or dressing requirements confirmed by the evaluating physician at 2 consecutive study visits 2 weeks apart
2 At this visit the subject will perform the EOS evaluation and enter the follow-up phase of the study
Study Visit 12EOS
1 If the study wound closes prior to the 12-week study mark subjects will perform EOS visit at the time of wound closure See Study Visit - Wound Closed
2 A subject whose wound does not close completely by week 12 will exited from the study after the week 12 wound evaluation
3 Document study compliance information from the subject
1 Amount of time the sock was worn throughout the week
2 Was it worn during the daynight
3 Whenwhy the sock was changed
4 Has the sock been on in the 3 hours leading up to the appointment
4 Remove sock and dressing and immediately perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed
5 Assess target ulcer if wound has closed document as such perform steps 7-12 and skip to Study Visit - Wound Closed
6 Perform standardized photography of the study wound
7 Assess the ulcer area cm2 perimeter cm and greatest depth cm using the inSight device
8 Perform SPP if wound is active or closed
9 Perform tcpO2 if wound is active or closed
10 Perform pain assessment
11 Ask the subject if they thought they were in the active or control group
12 Administer DFS-SF
13 Collect all relevant concomitant medication
14 Redress the wound per physician-directed standard of care
Study Visit Follow up
1 If the subjects wound closes within the 12-week treatment window they will enter the follow up phase of the study
2 At 3 months post closure wound evaluation will be performed as outlined below This followup visit will be in person In the event that an in-person visit is not possible a telehealth visit may be performed and documented as such
a Assess the study wound to determine that it remained closed b If the study wound has reoccurred i record the date of reoccurrence ii measure the size of dehiscence or re-ulceration iii exit the subject from the follow up phase c Assess the study foot for new sites of ulceration i record the date of reoccurrence ii measure the size of dehiscence or re-ulceration iii exit the subject from the follow up phase
Patients who present to the investigators institution through clinic admission direct transfer from another facility or through the emergency room may be recruited to participate in the study No direct marketing for subject recruitment will be done
Patients approached for study participation will be at least 22 years of age at the time of consent will undergo wound assessment and meet all eligibility requirements Those meeting eligibility criteria for the study will have the study explained to them by the Investigator An Informed Consent Form will be provided to sign according to Section 11 prior to undergoing any study procedures Patients will be encouraged to ask questions of the investigators It will be made clear to the patient that not participating in the study will in no way influence the treatment plan or the relationship with the physician
Wound Selection
Only one wound per subject will be included in the study Subjects with multiple wounds will have each wound measured for volume The wound with the largest volume meeting all eligibility requirements will be chosen for inclusion in the study The etiology of the chosen wound and if it is a new or recurring will be documented
Randomization and Blinding Procedure
Prior to study initiation Active and Control samples will be prepared in sealed and labeled as A or B also randomization envelopes will be provided to the research staff and used to obtain randomization assignment Within each randomization envelope there is an assignment of A or B After run-in evaluation the subjects wound will be debrided and dressed with SOC At the end of the procedure subjects who continue to meet all inclusion and no exclusion criteria will be randomized in a 11 ratio to be treated with either Control or Celliant therapies stratified by wound size greater than size of 4 cm2 and study center Study staff will use the randomization number labels and sock assignment of socks A or B contained in the envelope The number will become the subject ID The research staff will note the randomization number and the treatment assignment letter A or B on the CRF The key indicating therapy assignments Active or Control will only be available to staff not directly involved in the study until after the subject has completed study activities
Visit Schedule
Study procedures for each phase of study are outlined below In a later section details on each study procedure are described including equipment designation
Screening
1 Explain purpose and nature of the study and obtain signature on the informed consent document
2 Screen the subject against protocol inclusion and exclusion criteria including all pertinent tests
1 ABI andtoe pressure
2 Ulcer History measurement and classification
3 Urine Pregnancy test if indicated
Baseline may be done as same day as screening procedures
1 Obtain general medical history and demographic information and social history
2 Complete a physical examination body weight height and vital signs including measurement of resting heart rate respiratory rate and blood pressure while seated
3 Select the target ulcer
4 Obtain complete history pertinent to DFU disease including duration of the target ulcer previous and current treatment
5 Perform debridement if indicated Debridement is to be performed using curette scissors scalpel or forceps
6 Perform standardized photography and measurement of the study wound eKare or available camera with ruler Assess the post-debridement ulcer area cm2 perimeter cm and greatest depth cm using the inSight device eKare Fairfax VA These values are the baseline measurements for assessing accelerated wound closure at the two-week run-in visit
7 Perform baseline SPP note - this procedure does not need to be performed at baseline visit and can be performed at any visit through Run-In week 2Therapy initiation visit
8 Perform baseline tcpO2 note - this procedure does not need to be performed at baseline visit and can be performed at any visit through Run-In week 2Therapy initiation visit
9 Perform baseline hyperspectral imaging assessment on the dorsal and plantar aspects of the foot
10 Perform neuropathy and pain assessment
11 Obtain blood for hematology blood chemistry etc that were not covered in inclusionexclusion studies
12 Subjects who do not meet eligibility and fail to qualify to enter the Run-in will be deemed Screen failures and discharged noting the reasons for disqualification
13 Collect all relevant concomitant medication antibiotics antifungals and other anti-infective therapies
14 Wounds will be dressed SOC and offloaded per physician discretion
15 Subjects who qualify to enter the run-in will be instructed to refrain from using excluded medications and return to the office for Run-in Visit 2 within 7 1 days
Run-In ProceduresTherapy Initiation
Week 1 Run-in
1 Assess target ulcer
2 Perform debridement if indicated Debridement is to be performed using a curette scissors scalpel or forceps
3 Perform standardized photography of the study wound
4 Assess the post-debridement ulcer area cm2 perimeter cm and greatest depth cm using the inSight device
5 If wound size ulcer area increasesdecreases by 30 or more patient will be deemed a screen failure and removed from the study
6 If wound size ulcer area decreases by less than 30 patient wound will be treated with standard of care and return for run-in Week 2 Run-In within 7 1 days
7 Perform hyperspectral imaging assessment on the dorsal and plantar aspects of the foot
8 Perform pain assessment
9 Collect all relevant concomitant medication antibiotics antifungals and other anti-infective therapies
10 Wounds will be dressed SOC and offloaded per physician discretion
Week 2 Run-inTherapy Initiation
1 Assess target ulcer
2 Perform debridement if indicated Debridement is to be performed using curette scissors scalpel or forceps
3 Perform standardized photography of the study wound
4 Assess the post-debridement ulcer area cm2 perimeter cm and greatest depth cm using the inSight device
5 If wound size ulcer area increasesdecreases by 30 or more patient will be deemed a screen failure and removed from the study
6 If wound size ulcer area increasesdecreases by less than 30 patient wound will enter the study and randomized to either the Celliant Active or Control treatment arm
7 Perform hyperspectral imaging of the dorsal and plantar aspects of the foot
8 Perform pain assessment
9 Collect all relevant concomitant medication
10 Wound will be dressed with SOC and either Celliant Active or Control Sock applied
11 Wound will be offloaded
12 Provide subject with any additional medical socks needed until the next visit Instruct the subject to change the socks if they become wet soiled or bloody and under any conditions dictated by PI instructions
TherapyTreatment Phase
Study Visit 1-11
1 Document study compliance information from the subject
1 Amount of time the sock was worn throughout the week
2 Was it worn during the daynight
3 Whenwhy the sock was changed
4 Has the sock been on in the 3 hours leading up to the appointment
2 Remove sock and dressing and immediately perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed
3 Assess target ulcer if wound has closed document as such perform steps 7 and 8 and skip to Study Visit - Wound Closed
4 Debridement is to be performed if indicated using curette scissors scalpel or forceps If debridement is necessary at weekly visits all therapy must be removed and replaced post-debridement
5 Perform standardized photography of the study wound
6 Assess the ulcer area cm2 perimeter cm and greatest depth cm using the inSight device - if the wound is deemed closed by the physician skip to EOS visit
7 Perform SPP and tcPO2 measurements at Visit 4 maybe be taken instead at visit 5 or 6 if subject has not been wearing their treatment sock leading up to the visit or misses this visit
8 Collect all relevant concomitant medication
9 Perform pain assessment
10 Redress the wound with standard of care if wound is still active and apply Celliant Active or Control Sock and apply offloading if indicated
11 Wound will be offloaded
12 Provide subject with any additional medical socks needed until the next visit Instruct the subject to change the socks if they become wet soiled or bloody and under any conditions dictated by PI instructions Instruct the subject that they must wear the sock at all times and that including the 3 hours leading up to the next study visit
Study Visit - Wound Closed
1 The study wound is defined as closed when there is complete skin re-epithelialization without drainage or dressing requirements confirmed by the evaluating physician at 2 consecutive study visits 2 weeks apart
2 At this visit the subject will perform the EOS evaluation and enter the follow-up phase of the study
Study Visit 12EOS
1 If the study wound closes prior to the 12-week study mark subjects will perform EOS visit at the time of wound closure See Study Visit - Wound Closed
2 A subject whose wound does not close completely by week 12 will exited from the study after the week 12 wound evaluation
3 Document study compliance information from the subject
1 Amount of time the sock was worn throughout the week
2 Was it worn during the daynight
3 Whenwhy the sock was changed
4 Has the sock been on in the 3 hours leading up to the appointment
4 Remove sock and dressing and immediately perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed
5 Assess target ulcer if wound has closed document as such perform steps 7-12 and skip to Study Visit - Wound Closed
6 Perform standardized photography of the study wound
7 Assess the ulcer area cm2 perimeter cm and greatest depth cm using the inSight device
8 Perform SPP if wound is active or closed
9 Perform tcpO2 if wound is active or closed
10 Perform pain assessment
11 Ask the subject if they thought they were in the active or control group
12 Administer DFS-SF
13 Collect all relevant concomitant medication
14 Redress the wound per physician-directed standard of care
Study Visit Follow up
1 If the subjects wound closes within the 12-week treatment window they will enter the follow up phase of the study
2 At 3 months post closure wound evaluation will be performed as outlined below This followup visit will be in person In the event that an in-person visit is not possible a telehealth visit may be performed and documented as such
a Assess the study wound to determine that it remained closed b If the study wound has reoccurred i record the date of reoccurrence ii measure the size of dehiscence or re-ulceration iii exit the subject from the follow up phase c Assess the study foot for new sites of ulceration i record the date of reoccurrence ii measure the size of dehiscence or re-ulceration iii exit the subject from the follow up phase
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
True
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None