Ignite Creation Date:
2024-05-06 @ 3:09 PM
Last Modification Date:
2024-10-26 @ 1:43 PM
Study NCT ID:
NCT04535804
Status:
UNKNOWN
Last Update Posted:
2020-09-02
First Post:
2020-08-27
Brief Title:
Aspirin in the Treatment of Pregnant Women With Adenomyosis on Reducing Preterm Delivery
Sponsor:
Shanghai First Maternity and Infant Hospital
Organization:
Shanghai First Maternity and Infant Hospital
Study Overview
Official Title:
Clinical Randomized Controlled Trial of Aspirin in the Treatment of Pregnant Women With Adenomyosis on Reducing Preterm Delivery
Status:
UNKNOWN
Status Verified Date:
2020-08
Last Known Status:
NOT_YET_RECRUITING
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:
None
Brief Summary:
Objective This study intends to carry out a randomized double-blind clinical trial study of aspirin in the treatment of pregnancy with adenomyosis to reduce the incidence of preterm delivery and provide a new therapeutic target for the prevention and treatment of premature birth and adverse pregnancy outcomes and fill in the blank of effective prevention of premature delivery in pregnancy with adenomyosis at home and abroad Application value and social and economic benefits of the bed
Methods a randomized double-blind clinical trial was used in this study In Shanghai first maternal and child health care hospital the pregnant women who meet the requirements of the group will be given full informed consent By using a random double-blind research method 1-550 digital computers are randomly divided into two groups with two groups of digital coding placebo and aspirin From 12 weeks of gestation 100 mg of placebo or low-dose aspirin was given orally 2 tablets a time twice a day before going to bed to 36 weeks of gestation
Observe the outcome ① Main outcome measures preterm delivery delivery less than 37 weeks gestational weeks premature delivery The specific classification includes A extremely premature delivery gestational age 28-32 weeks B early preterm birth delivery gestational weeks 32-34 gestational weeks C late preterm birth 34-36 gestational weeks
② Secondary outcome measures abortion gestational diabetes mellitus gestational hypertension placental disorders SGA FGR premature rupture of membranes postpartum hemorrhage mode of delivery etc
The follow-up contents were as follows
Routine prenatal examination blood pressure fetal size vaginal bleeding etc
Coagulation factor index prothrombin time Pt activated partial thrombin time APTT thrombin time TT fibrinogen FIB D-dimer
Immune related indexes antiphospholipid antibody CA125 ④ Inflammatory index routine blood test CRP
Detection of cervical length by B-ultrasound ⑥ Pregnancy complications gestational diabetes mellitus gestational hypertension and placental disorders ⑦ Birth outcome gestational weeks birth weight FGR premature delivery mode of delivery NICU rate etc
Methods a randomized double-blind clinical trial was used in this study In Shanghai first maternal and child health care hospital the pregnant women who meet the requirements of the group will be given full informed consent By using a random double-blind research method 1-550 digital computers are randomly divided into two groups with two groups of digital coding placebo and aspirin From 12 weeks of gestation 100 mg of placebo or low-dose aspirin was given orally 2 tablets a time twice a day before going to bed to 36 weeks of gestation
Observe the outcome ① Main outcome measures preterm delivery delivery less than 37 weeks gestational weeks premature delivery The specific classification includes A extremely premature delivery gestational age 28-32 weeks B early preterm birth delivery gestational weeks 32-34 gestational weeks C late preterm birth 34-36 gestational weeks
② Secondary outcome measures abortion gestational diabetes mellitus gestational hypertension placental disorders SGA FGR premature rupture of membranes postpartum hemorrhage mode of delivery etc
The follow-up contents were as follows
Routine prenatal examination blood pressure fetal size vaginal bleeding etc
Coagulation factor index prothrombin time Pt activated partial thrombin time APTT thrombin time TT fibrinogen FIB D-dimer
Immune related indexes antiphospholipid antibody CA125 ④ Inflammatory index routine blood test CRP
Detection of cervical length by B-ultrasound ⑥ Pregnancy complications gestational diabetes mellitus gestational hypertension and placental disorders ⑦ Birth outcome gestational weeks birth weight FGR premature delivery mode of delivery NICU rate etc
Detailed Description:
Research background
Adenomyosis AD is a benign uterine disease with endometrial glands and stroma invading into the myometrium accompanied by hyperplasia and hypertrophy of uterine smooth muscle cells which leads to abnormal uterine structure and function In non pregnancy period the main manifestations are diffuse enlargement of uterus dysmenorrhea menorrhagia menorrhagia which can lead to infertility In recent years with the delay of childbearing age the incidence of adenomyosis in pregnancy is increasing gradually The incidence of adenomyosis in the general population reached 209 while the incidence of adenomyosis was higher in recurrent abortion and assisted reproduction reaching 382 and 347 respectively Studies have shown that adenomyosis is associated with early preterm delivery late preterm delivery low birth weight infants very low birth weight infants and small for gestational age infants Patients with adenomyosis are prone to hypertensive disorder complicating pregnancy intrauterine infection abnormal placenta and increased cesarean section postpartum hemorrhage and abnormal fetal position
Aspirin is widely used in the treatment of immune system diseases and the prevention of cerebrovascular diseases because of its anti-inflammatory and anti platelet aggregation effects Aspirin is more and more widely used in obstetrics and Gynecology such as recurrent abortion caused by antiphospholipid antibody syndrome recurrent abortion related to abnormal uterine artery blood flow and unexplained recurrent abortion Since 1980 aspirin has been widely recommended for the prevention of pregnancy with high risk factors of preeclampsia and intrauterine growth restriction and it has been confirmed that aspirin is effective in the prevention of pregnancy It is safe in clinical application The inflammatory environment of adenomyosis is closely related to the initiation of preterm delivery but whether aspirin can benefit pregnant women with adenomyosis is still lacking
Research plan
1 Study population Inclusive criteria ① Singleton ② in line with the diagnosis of adenomyosis in pregnancy ③ no history of chronic diseases and definite diagnosis of endocrine diseases including diabetes hypertension obesity antiphospholipid syndrome ④ informed consent and voluntary participation in this study
Exclusion criteria ① twins multiple births ② induced labor for medical reasons ③ allergic to aspirin or other salicylates tetracycline drugs or any other components of drugs ④ patients with mental disorders ⑤ transferred to hospital
Withdrawal criteria Subjects withdraw informed consent subjects request to withdraw from the trial
Termination of the experiment unacceptable adverse events occurred the subjects voluntarily asked to withdraw from the trial the protocol was violated the researcher ethics committee considered it necessary for the subjects to stop the trial
2 Diagnostic criteria of adenomyosis according to pre pregnancy and early pregnancy transvaginal ultrasound diagnosis The diagnostic criteria of transvaginal ultrasound for adenomyosis include a ectopic endometrial glands and stroma b myometrium hyperplasia hypertrophy and increased blood vessels
3 Sample size calculation the incidence of preterm delivery in pregnant women with adenomyosis was about 2163 Mette R Bruun et al 2018 It is expected that the incidence of preterm birth in patients with adenomyosis during pregnancy will be reduced by 40 after aspirin intervention that is the incidence of premature delivery in the intervention group will be about 1298 Assuming that the test level α is 005 the test efficiency is 08 and one-sided test 236 sample sizes are estimated for the intervention group and the control group by using the sample size estimation software pass Considering the loss of follow-up rate of about 10 the sample size of intervention group and control group was about 262 cases Therefore 550 pregnant women were recruited in this study
4 Statistical analysis plan the statistical analysis in the study is based on the principle of intention to treat ITT that is all the subjects involved in the study participate in the statistical analysis Chi square test or unpaired t test was used to analyze the difference between the intervention group and the control group In the chi square test if the theoretical frequency of cells was less than 5 Fisher exact probability method was used and the Mann Whitney U test was used for quantitative variables that did not conform to normal distribution Chi square test was used to analyze the difference of preterm birth rate between intervention group and control group Logistic regression model was used to estimate the relative risk value and 95 confidence interval 95 confidence interval of preterm birth between the two groups The choice of statistical analysis method for secondary outcome indicators was consistent with that in primary outcome analysis SAS viya was used as the analysis software in the study and the difference was statistically significant when p 005
research implementation process research steps describe the data collection content and method according to the time node 202010-202012we distributed recruitment advertisements prepared placebos and aspirin screened and enrolled patients signed informed consent and arranged outpatient follow-up of enrolled patients 202101-202106150 cases of pregnant women with adenomyosis were planned to be enrolled and the registration and follow-up of the patients were done well 202107-202112150 cases of pregnant women with adenomyosis were planned to be enrolled the experimental data were summarized gradually the information of defect was recorded 202201-202206150 cases of pregnancy with adenomyosis were planned to be enrolled the pregnancy outcomes of the pregnant women were counted and the case report forms were completed 202207-202209 we plan to complete the work of 50 cases of pregnancy with adenomyosis analyze the data statistically write papers and final reports
Risk of study placebo had no effect on subjects adverse reactions of aspirin mainly included gastrointestinal reactions risk of fetal teratogenesis before 12 weeks of pregnancy and risk of bleeding during pregnancy However since 1980 aspirin has been widely used in the prevention of pregnancy with high risk factors of preeclampsia and fetal growth restriction which proves that the probability of adverse reactions of low-dose aspirin is very low no teratogenic effect is found and it has clinical safety
Benefits of the study expected to reduce the incidence of preterm birth and improve adverse pregnancy outcomes In order to explore the prevention and treatment of premature delivery and adverse pregnancy outcomes it is necessary to provide a new therapeutic target fill in the blank of the effective prevention of premature birth treatment of pregnancy combined with adenomyosis at home and abroad which may reduce the medical costs related to pregnancy complications and adverse pregnancy outcomes as well as the cost of dealing with adverse pregnancy outcomes This study has important clinical application value and social and economic benefits
Recruitment and protection measures of subjects There are recruitment advertisements in this study and other documents are provided Protective measures for the subjects in order to reduce the adverse reactions of aspirin as far as possible we used aspirin enteric coated tablets 50mg twice a day the dosage belongs to low dose From 12 weeks of gestation to 36 weeks of gestation If you have bleeding during pregnancy you need to stop taking aspirin and you can continue to take aspirin after the bleeding disappears The number of follow-up visits during pregnancy is roughly the same as that of general prenatal examination about 10 times without additional visits about 5ml more blood will be drawn for examination on the day of establishing pregnancy card and the extra examination cost will be borne by the research group we will arrange experienced doctors to take charge of the whole pregnancy examination of the subjects and keep communication at any time We will pay more attention to the subjects gastrointestinal reaction tinnitus erythema liver and kidney function and other discomfort during each birth examination If there is any abnormality we will take the following measures 1 immediately stop your experiment if the condition requires 2 be responsible for the treatment of your adverse drug reactions 3 give appropriate economic compensation according to the degree of your injury
Informed consent process the subjects informed consent work is in charge of a specially assigned person who will provide sufficient and easy to understand information to the pregnant women who meet the inclusion conditions the subjects of informed consent are all those with independent ability and they will not be able to participate in this project if they have no independent ability there will be no pressure on pregnant women who meet the inclusion conditions in the process of informed consent In the process of participating in the research it will ensure that research participants get timely information including their rights safety and health
Adenomyosis AD is a benign uterine disease with endometrial glands and stroma invading into the myometrium accompanied by hyperplasia and hypertrophy of uterine smooth muscle cells which leads to abnormal uterine structure and function In non pregnancy period the main manifestations are diffuse enlargement of uterus dysmenorrhea menorrhagia menorrhagia which can lead to infertility In recent years with the delay of childbearing age the incidence of adenomyosis in pregnancy is increasing gradually The incidence of adenomyosis in the general population reached 209 while the incidence of adenomyosis was higher in recurrent abortion and assisted reproduction reaching 382 and 347 respectively Studies have shown that adenomyosis is associated with early preterm delivery late preterm delivery low birth weight infants very low birth weight infants and small for gestational age infants Patients with adenomyosis are prone to hypertensive disorder complicating pregnancy intrauterine infection abnormal placenta and increased cesarean section postpartum hemorrhage and abnormal fetal position
Aspirin is widely used in the treatment of immune system diseases and the prevention of cerebrovascular diseases because of its anti-inflammatory and anti platelet aggregation effects Aspirin is more and more widely used in obstetrics and Gynecology such as recurrent abortion caused by antiphospholipid antibody syndrome recurrent abortion related to abnormal uterine artery blood flow and unexplained recurrent abortion Since 1980 aspirin has been widely recommended for the prevention of pregnancy with high risk factors of preeclampsia and intrauterine growth restriction and it has been confirmed that aspirin is effective in the prevention of pregnancy It is safe in clinical application The inflammatory environment of adenomyosis is closely related to the initiation of preterm delivery but whether aspirin can benefit pregnant women with adenomyosis is still lacking
Research plan
1 Study population Inclusive criteria ① Singleton ② in line with the diagnosis of adenomyosis in pregnancy ③ no history of chronic diseases and definite diagnosis of endocrine diseases including diabetes hypertension obesity antiphospholipid syndrome ④ informed consent and voluntary participation in this study
Exclusion criteria ① twins multiple births ② induced labor for medical reasons ③ allergic to aspirin or other salicylates tetracycline drugs or any other components of drugs ④ patients with mental disorders ⑤ transferred to hospital
Withdrawal criteria Subjects withdraw informed consent subjects request to withdraw from the trial
Termination of the experiment unacceptable adverse events occurred the subjects voluntarily asked to withdraw from the trial the protocol was violated the researcher ethics committee considered it necessary for the subjects to stop the trial
2 Diagnostic criteria of adenomyosis according to pre pregnancy and early pregnancy transvaginal ultrasound diagnosis The diagnostic criteria of transvaginal ultrasound for adenomyosis include a ectopic endometrial glands and stroma b myometrium hyperplasia hypertrophy and increased blood vessels
3 Sample size calculation the incidence of preterm delivery in pregnant women with adenomyosis was about 2163 Mette R Bruun et al 2018 It is expected that the incidence of preterm birth in patients with adenomyosis during pregnancy will be reduced by 40 after aspirin intervention that is the incidence of premature delivery in the intervention group will be about 1298 Assuming that the test level α is 005 the test efficiency is 08 and one-sided test 236 sample sizes are estimated for the intervention group and the control group by using the sample size estimation software pass Considering the loss of follow-up rate of about 10 the sample size of intervention group and control group was about 262 cases Therefore 550 pregnant women were recruited in this study
4 Statistical analysis plan the statistical analysis in the study is based on the principle of intention to treat ITT that is all the subjects involved in the study participate in the statistical analysis Chi square test or unpaired t test was used to analyze the difference between the intervention group and the control group In the chi square test if the theoretical frequency of cells was less than 5 Fisher exact probability method was used and the Mann Whitney U test was used for quantitative variables that did not conform to normal distribution Chi square test was used to analyze the difference of preterm birth rate between intervention group and control group Logistic regression model was used to estimate the relative risk value and 95 confidence interval 95 confidence interval of preterm birth between the two groups The choice of statistical analysis method for secondary outcome indicators was consistent with that in primary outcome analysis SAS viya was used as the analysis software in the study and the difference was statistically significant when p 005
research implementation process research steps describe the data collection content and method according to the time node 202010-202012we distributed recruitment advertisements prepared placebos and aspirin screened and enrolled patients signed informed consent and arranged outpatient follow-up of enrolled patients 202101-202106150 cases of pregnant women with adenomyosis were planned to be enrolled and the registration and follow-up of the patients were done well 202107-202112150 cases of pregnant women with adenomyosis were planned to be enrolled the experimental data were summarized gradually the information of defect was recorded 202201-202206150 cases of pregnancy with adenomyosis were planned to be enrolled the pregnancy outcomes of the pregnant women were counted and the case report forms were completed 202207-202209 we plan to complete the work of 50 cases of pregnancy with adenomyosis analyze the data statistically write papers and final reports
Risk of study placebo had no effect on subjects adverse reactions of aspirin mainly included gastrointestinal reactions risk of fetal teratogenesis before 12 weeks of pregnancy and risk of bleeding during pregnancy However since 1980 aspirin has been widely used in the prevention of pregnancy with high risk factors of preeclampsia and fetal growth restriction which proves that the probability of adverse reactions of low-dose aspirin is very low no teratogenic effect is found and it has clinical safety
Benefits of the study expected to reduce the incidence of preterm birth and improve adverse pregnancy outcomes In order to explore the prevention and treatment of premature delivery and adverse pregnancy outcomes it is necessary to provide a new therapeutic target fill in the blank of the effective prevention of premature birth treatment of pregnancy combined with adenomyosis at home and abroad which may reduce the medical costs related to pregnancy complications and adverse pregnancy outcomes as well as the cost of dealing with adverse pregnancy outcomes This study has important clinical application value and social and economic benefits
Recruitment and protection measures of subjects There are recruitment advertisements in this study and other documents are provided Protective measures for the subjects in order to reduce the adverse reactions of aspirin as far as possible we used aspirin enteric coated tablets 50mg twice a day the dosage belongs to low dose From 12 weeks of gestation to 36 weeks of gestation If you have bleeding during pregnancy you need to stop taking aspirin and you can continue to take aspirin after the bleeding disappears The number of follow-up visits during pregnancy is roughly the same as that of general prenatal examination about 10 times without additional visits about 5ml more blood will be drawn for examination on the day of establishing pregnancy card and the extra examination cost will be borne by the research group we will arrange experienced doctors to take charge of the whole pregnancy examination of the subjects and keep communication at any time We will pay more attention to the subjects gastrointestinal reaction tinnitus erythema liver and kidney function and other discomfort during each birth examination If there is any abnormality we will take the following measures 1 immediately stop your experiment if the condition requires 2 be responsible for the treatment of your adverse drug reactions 3 give appropriate economic compensation according to the degree of your injury
Informed consent process the subjects informed consent work is in charge of a specially assigned person who will provide sufficient and easy to understand information to the pregnant women who meet the inclusion conditions the subjects of informed consent are all those with independent ability and they will not be able to participate in this project if they have no independent ability there will be no pressure on pregnant women who meet the inclusion conditions in the process of informed consent In the process of participating in the research it will ensure that research participants get timely information including their rights safety and health
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