Determine the effect of prescribing of misoprostol in reducing postpartum pregnancy and delivery success

Phase 3

• Conditions: Post-term Pregnancy.; Post-term pregnancy; O48.0

• Registration Number: IRCT20180215038742N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

Pregnant women with gestational age 39 weeks
Primigravida
Between 18 - 40 years old
Singletone pregnancy
Normal fetal heart rate
Cephalic presentation (Vertex)
AFI equal or more than 5 cm
No history of medical or midwifery disorders
Bishop score less than 8
Reactive NST
Without uterine contractions

Exclusion Criteria

Macrosomia
Sensitivity to PGs
Uterin wall scar
Preeclampsia or blood pressure more than 140/90 mmhg
PROM
Vaginal Bleeding
IUGR fetus

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Delivery rate before 41th week of gestational age. Timepoint: 39th week, 40th week and then every other day. Method of measurement: newborn birth.