Different Types of Progesterone in the Prevention of Preterm Labor
Primary Purpose
Preterm Labor
Status
Unknown status
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
17 alpha hydroxyprogestrone caproate
Vaginal progesterone
Oral dydrogesterone
Sponsored by
About this trial
This is an interventional prevention trial for Preterm Labor
Eligibility Criteria
Inclusion Criteria:
- Singleton pregnancy
- Living fetus with gestational age 16-18weeks (calculated according to date of last menstrual period confirmed with earlier ultrasound examination).
Presence of risk factor for preterm labor:
- Previous spontaneous preterm labor in previous singleton Pregnancy, OR
- Previous spontaneous second trimestric miscarriage less than 3 times, OR
- Short cervix less than 25mm diagnosed during midtrimesteric transvaginal ultrasound examination at 16-18 weeks with or without history of previous preterm labor.
Exclusion Criteria:
- Multiple pregnancy.
- Medical or obstetric conditions requiring termination of pregnancy
Contraindication to progesterone administration or its use earlier in this pregnancy
- Current or past history of thrombophlebitis, thromboembolic disorders, or cerebral apoplexy.
- Liver dysfunction or disease.
- Known or suspected malignancy of breast or genital organs.
- Undiagnosed vaginal bleeding.
- Missed abortion.
- Known sensitivity to progesterone injection.
- Known sensitivity to sesame oil/seeds.
- Congenital fetal anomalies
- Cervical cerclage in the current pregnancy.
- Presence of uterine anomalies (Unicornuate uterus , Uterus didelphys, bicornuate uterus,Septated uterus) or uterine fibroid.
- Presence of history of chronic hypertetion, chronic liver or kidney diseases, and pregnancy induced hypertension.
Sites / Locations
- Ain SHams Maternity HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
17 alpha hydroxyprogestrone caproate Group
Vaginal progesterone Group
Oral dydrogesterone Group
Arm Description
Patients will receive 250 mg of 17 alpha hydroxyprogestrone caproate intramuscularly once weekly starting from 16 weeks till delivery or 36 weeks.
Patients will receive vaginal progesterone 200 mg once per day starting from 16 weeks till delivery or 36 weeks.
Patients will receive 2 tablets of oral dydrogesterone daily starting from 16 weeks till delivery or 36 weeks
Outcomes
Primary Outcome Measures
Gestational age in weeks at delivery.
using either the last menstrual period in patients with regular cycles or early first trimester ultrasound to calculate the gestational age in weeks at delivery
Secondary Outcome Measures
Hemodynamic changes in fetoplacental circulation
Measurement of U/S Doppler indices of umbilical artery and middle cerebral artery (namely PI, RI and S/D ratio) in fetal circulation
Unsatisfactory response
Number of patients who needed to increase the dose above the recommended initial dose.
Failure of prevention of preterm labor
Number of patients who suffered preterm labor and needed tocolysis
Birth weight
Birth weight in Kg
Neonatal APGAR score
Neonatal Apgar score at 1 and 5 min.
Need for NICU admission
Number of patients whose neonates were admitted to NICU
Neonatal mortality.
Neonatal mortality
Number of neonatal deaths
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03537287
Brief Title
Different Types of Progesterone in the Prevention of Preterm Labor
Official Title
Intramuscular 17Alpha-hydroxyprogestrone, Progesterone Suppositories and Dydrogesterone Tablets in Preventing Preterm Labor
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 2016 (Actual)
Primary Completion Date
July 2018 (Anticipated)
Study Completion Date
August 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Preterm birth is a common problem in obstetric care,with estimates ranging from 5% in several European countries to 18% in some African countries, Preterm labor defined as delivery before 37 completed weeks is the leading cause of perinatal and neonatal morbidity and mortality and strongly related to the developmental and neurological disabilities later in life..
There is still considerable uncertainty regarding the optimal progesterone type, route of administration, dosage and timing of start of therapy to prevent preterm labor in risky women
Detailed Description
This study aims to compare between the efficacy of intramuscular 17alpha-hydroxyprogestrone, progesterone vaginal suppositories and dydrogesterone oral tablets in prevention of preterm labor in high risk women.
All women will be counseled regarding mode of intervention and informed consent will be obtained. All cases will be subjected to complete history taking, routine antenatal examination and investigations, treatment of genital or urinary tract infections if diagnosed. Routine obstetric ultrasound examination and measurement of cervical length by transvaginal ultrasound will be carried out at 16-18weeks of pregnancy.
The study population will be randomly distributed according to the mode of intervention into 3 groups.
Randomization is performed using a Computer-generated randomization system. Blinding of the intervention is not feasible in this trial (owing to the different route of administration of the studied drugs).Table of randomization is obtained
Group 1:
Women who will take intramuscular 17 alpha hydroxyprogestrone caproate
Dose:
250 mg intramuscularly, once weekly starting from 16 weeks till delivery or 36 weeks.
Group 2 :
Women who will take progesterone 200mg vaginal suppositories.
Dose:
Once per day starting from 16 weeks till delivery or 36 weeks
Group 3 :
Women who will take oral dydrogesterone
Dose:
Take 2 tablets a day starting from 16 weeks till delivery or 36 weeks
Color Doppler blood flow velocity examination of fetal circulation will be performed by an independent investigator blinded to treatment before treatment &after two weeks of treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Labor
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
17 alpha hydroxyprogestrone caproate Group
Arm Type
Active Comparator
Arm Description
Patients will receive 250 mg of 17 alpha hydroxyprogestrone caproate intramuscularly once weekly starting from 16 weeks till delivery or 36 weeks.
Arm Title
Vaginal progesterone Group
Arm Type
Active Comparator
Arm Description
Patients will receive vaginal progesterone 200 mg once per day starting from 16 weeks till delivery or 36 weeks.
Arm Title
Oral dydrogesterone Group
Arm Type
Active Comparator
Arm Description
Patients will receive 2 tablets of oral dydrogesterone daily starting from 16 weeks till delivery or 36 weeks
Intervention Type
Drug
Intervention Name(s)
17 alpha hydroxyprogestrone caproate
Intervention Description
250 mg of 17 alpha hydroxyprogestrone caproate weekly
Intervention Type
Drug
Intervention Name(s)
Vaginal progesterone
Intervention Description
200 mg of vaginal progesterone daily
Intervention Type
Drug
Intervention Name(s)
Oral dydrogesterone
Intervention Description
2 tablets of dydrogesterone daily
Primary Outcome Measure Information:
Title
Gestational age in weeks at delivery.
Description
using either the last menstrual period in patients with regular cycles or early first trimester ultrasound to calculate the gestational age in weeks at delivery
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Hemodynamic changes in fetoplacental circulation
Description
Measurement of U/S Doppler indices of umbilical artery and middle cerebral artery (namely PI, RI and S/D ratio) in fetal circulation
Time Frame
6 months
Title
Unsatisfactory response
Description
Number of patients who needed to increase the dose above the recommended initial dose.
Time Frame
6 months
Title
Failure of prevention of preterm labor
Description
Number of patients who suffered preterm labor and needed tocolysis
Time Frame
6 months
Title
Birth weight
Description
Birth weight in Kg
Time Frame
6 months
Title
Neonatal APGAR score
Description
Neonatal Apgar score at 1 and 5 min.
Time Frame
6 months
Title
Need for NICU admission
Description
Number of patients whose neonates were admitted to NICU
Neonatal mortality.
Time Frame
6 months
Title
Neonatal mortality
Description
Number of neonatal deaths
Time Frame
6 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Singleton pregnancy
Living fetus with gestational age 16-18weeks (calculated according to date of last menstrual period confirmed with earlier ultrasound examination).
Presence of risk factor for preterm labor:
Previous spontaneous preterm labor in previous singleton Pregnancy, OR
Previous spontaneous second trimestric miscarriage less than 3 times, OR
Short cervix less than 25mm diagnosed during midtrimesteric transvaginal ultrasound examination at 16-18 weeks with or without history of previous preterm labor.
Exclusion Criteria:
Multiple pregnancy.
Medical or obstetric conditions requiring termination of pregnancy
Contraindication to progesterone administration or its use earlier in this pregnancy
Current or past history of thrombophlebitis, thromboembolic disorders, or cerebral apoplexy.
Liver dysfunction or disease.
Known or suspected malignancy of breast or genital organs.
Undiagnosed vaginal bleeding.
Missed abortion.
Known sensitivity to progesterone injection.
Known sensitivity to sesame oil/seeds.
Congenital fetal anomalies
Cervical cerclage in the current pregnancy.
Presence of uterine anomalies (Unicornuate uterus , Uterus didelphys, bicornuate uterus,Septated uterus) or uterine fibroid.
Presence of history of chronic hypertetion, chronic liver or kidney diseases, and pregnancy induced hypertension.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohamed Samy, MD
Phone
01001947488
Email
mohammedsamy8132@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed Samy, MD
Organizational Affiliation
M Samy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ain SHams Maternity Hospital
City
Cairo
State/Province
Abbaseya
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohamed Samy, MD
12. IPD Sharing Statement
Plan to Share IPD
No
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Different Types of Progesterone in the Prevention of Preterm Labor
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