PPROM.
Conditions
Interventions
Intervention 1: Intervention group: Recipients of rectal progesterone suppository 400 mg ( Abu Reihan Company production), once a day. Intervention 2: Control group: No therapeutic intervention.
Sponsors
Gorgan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Pregnant women 18-45 years Fetus age between 26-34 weeks based on first trimester of pregnancy ultrasound PPROM diagnosis based on observation of leakage during speculum examination, nitrazine positive test that these pregnant mothers PPROM without labor pain
Exclusion criteria
Exclusion criteria: Fetus chromosomal abnormalities Abnormal biophysical profiles less than 4 Intrauterine growth restriction and weight less than ten percent according to the Alexander Growth Standard Maternal fever greater than 38 ° C Bleeding after week 24 Chorioamnionitis based on maternal criteria Type 1 diabetes Preeclampsia includes high blood pressure and proteinuria after 20 weeks of pregnancy Cervical discharge and severe obstetric medical diseases Taking corticosteroids or systemic steroids Receive antibiotics one week before hospital admission and antibiotic sensitivity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increased latent phase of labor. Timepoint: From the beginning of the latent phase to the end of the latent phase. Method of measurement: Measurement of latent phase duration based on clinical examination.;Neonatal Apgar score. Timepoint: Apgar score of the first and fifth minutes after birth. Method of measurement: Based on Apgar scoring criteria. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Behnaz Gonabadi
Gorgan University of Medical Sciences
Outcome results
None listed