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NCT00432588 Clinical Trial

Comparing the Effect of Vaginal Misoprostol With Dinoprostone in Term Pregnancies

Preeclampsia Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT00432588
Other study ID # Misoprostol vs Dinoprostone
Secondary ID
Status Not yet recruiting
Phase Phase 1/Phase 2
First received February 6, 2007
Last updated May 31, 2007

Study information
Verified date February 2007
Source Hormozgan University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Hypothesis (H0): Labor duration and obstetric complications are not significantly different in the three groups (misoprostol-dinoprostone-oxytocin).

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Term pregnancy

- Singleton

- Vertex

- Bishop score below 6

Exclusion Criteria:

- History of drug reaction

- Medical disease

- IUGR

- Oligohydramnios

- Vaginal bleeding

- Fetal anomaly

- Uterine scar

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• misoprostol

• dinoprostone

Locations
Country Name City State
Iran, Islamic Republic of Shariaty Maternity Hospital Tehran

Sponsors (1)
Lead Sponsor Collaborator
Hormozgan University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

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