Trials / Completed
CompletedNCT06560515
Dinoprostone Versus Vaginal Misoprostol for Induction of Labour
Vaginal Dinoprostone Versus Vaginal Misoprostol for Induction of Labour in Post-dated Pregnancy; a Randomized Controlled Study.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 370 (actual)
- Sponsor
- University of Alexandria · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
This randomized controlled study was carried out on 370 pregnant women with gestational age ≥ 40 weeks of different ages and parities at El-Shatby Maternity University Hospital after approval of ethical committee of Alexandria Faculty of Medicine. After assessment for eligibility \& enrollment in the study, women were randomly assigned into one of the two study groups, Group (I) received 3 mg vaginal Dinoprostone of maximum 2 doses 6 hours apart and Group (II) received 50 μg of vaginal misoprostol of maximum 2 doses 6 hours apart.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Vaginal Dinoprostone | induction of labour in women with postdate pregnancy with vaginal dinoprostone vs. vaginal misoprostol |
Timeline
- Start date
- 2022-08-01
- Primary completion
- 2023-07-31
- Completion
- 2023-10-31
- First posted
- 2024-08-19
- Last updated
- 2024-08-19
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT06560515. Inclusion in this directory is not an endorsement.