Preterm Birth
Conditions
Keywords
Preterm Birth, Oral Micronized Progesterone
Brief summary
This is a randomized, double-blind, placebo-controlled study.
Detailed description
Intervention: The study subjects will be randomized to receive twice daily tablets of either 100 mg of OMP (Uterocare®, October Pharma , Sixth of October city, Egypt) or placebo from enrollment (14-18 weeks) until 36 weeks or delivery, whichever occurs first. The patients and medical staff will be blinded to the study medication allocation. Method of Randomization: All patients who are fit for admission into the study will pull one of the numbered sealed identical black bags containing either the active medicine (=25%), the placebo (with the aim of admission into data collection, =25%), or a placebo together with a short note explaining that they will not be admitted to the study (=50%) and that they can give back their bag to the head nurse. The code for the 424 (106x4) bag numbers is a confidential computer generated random number list (generated using MedCalc© Software bvba, Ostend, Belgium). It will be left, in a sealed envelope, with the head nurse of the antenatal clinic, till the end of data collection.ruptured membranes. 5\. Obstetric ultrasound for gestational age, amniotic fluid volume, fetal weight, placental position, fetal anomalies. 6\. Transvaginal ultrasound is not always available for cervical length assessment in ASUMH, so it will not be a necessary step in patients assessment but will be done whenever available. Follow up: Patients will be followed up regularly, at twice monthly intervals, in the antenatal clinic of Ain Shams University Maternity Hospital until delivery. They will be instructed to return to the hospital when recurrence of symptoms of preterm labor, rupture of membranes, or vaginal bleeding. There will be telephone call follow ups routinely to ensure adherence to the study protocol.
Interventions
DRUGmicronized progesterone
Oral
DRUGPlacebo
Oral
Sponsors
Ain Shams Maternity Hospital
Ghamra Military Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No
Inclusion criteria
1. Singleton pregnancies. 2. Gestational age, on admission, is between 14 and 18 weeks. 3. Past history of at least one idiopathic preterm birth.
Exclusion criteria
1. Established preterm labor (cervical dilatation ≥ 4 cm). 2. Persistent uterine contractions. 3. Women with medical or surgical complications indicating delivery or termination of pregnancy. 4. Presence of fetal anomalies incompatible with life. 5. Premature rupture of membranes.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The rate (incidence) of preterm delivery (gestational age <37 weeks). | up to 37weeks. | Patients will be followed up regularly, at twice monthly intervals, in the antenatal clinic of Ain Shams University Maternity Hospital until delivery. They will be instructed to return to the hospital when recurrence of symptoms of preterm labor, rupture of membranes, or vaginal bleeding. There will be telephone call follow up routinely to ensure adherence to the study protocol. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The incidence of rupture of the amniotic membranes. | up to 37weeks. | Patients will be followed up regularly, at twice monthly intervals, in the antenatal clinic of Ain Shams University Maternity Hospital until delivery. They will be instructed to return to the hospital when recurrence of symptoms of preterm labor, rupture of membranes, or vaginal bleeding. There will be telephone call follow up routinely to ensure adherence to the study protocol. |
| The neonatal birth weight | up to 37 weeks. | Patients will be followed up regularly, at twice monthly intervals, in the antenatal clinic of Ain Shams University Maternity Hospital until delivery. |
Countries
Egypt
Contacts
Primary Contactahmed A Abdel-Aziz
Outcome results
None listed