Preterm Labor
Conditions
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.
Interventions
DRUG17 alpha hydroxyprogestrone caproate
250 mg of 17 alpha hydroxyprogestrone caproate weekly
DRUGVaginal progesterone
200 mg of vaginal progesterone daily
2 tablets of dydrogesterone daily
Sponsors
Ain Shams University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No
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: 1. Previous spontaneous preterm labor in previous singleton Pregnancy, OR 2. Previous spontaneous second trimestric miscarriage less than 3 times, OR 3. 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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Gestational age in weeks at delivery. | 6 months | 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
| Measure | Time frame | Description |
|---|---|---|
| Unsatisfactory response | 6 months | Number of patients who needed to increase the dose above the recommended initial dose. |
| Failure of prevention of preterm labor | 6 months | Number of patients who suffered preterm labor and needed tocolysis |
| Birth weight | 6 months | Birth weight in Kg |
| Hemodynamic changes in fetoplacental circulation | 6 months | Measurement of U/S Doppler indices of umbilical artery and middle cerebral artery (namely PI, RI and S/D ratio) in fetal circulation |
| Need for NICU admission | 6 months | Number of patients whose neonates were admitted to NICU Neonatal mortality. |
| Neonatal mortality | 6 months | Number of neonatal deaths |
| Neonatal APGAR score | 6 months | Neonatal Apgar score at 1 and 5 min. |
Countries
Egypt
Contacts
Primary ContactMohamed Samy, MD
Outcome results
None listed