Trials / Completed
CompletedNCT01508143
Comparitive Study of Two Misoprostol Regimen in Early Pregnancy Termination
A Comparative Study of Vaginal Misoprostol Two Dosing Regimen for First Trimester Pregnancy Termination in Patients Admitted at Bandarabbas in Shariati Hospital in 2009
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 41 (actual)
- Sponsor
- Hormozgan University of Medical Sciences · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to compare two misoprostol regimen in pregnancy termination.
Detailed description
Studies on determining the optimal dosage for misoprostol in pregnancy termination are continuing and still there is no evidence for ideal misoprostol regimen for pregnancy termination. The aim of this study is to compare two misoprostol regimen in pregnancy termination.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol 400 micrograms | Misoprostol 400 micrograms each 6 hours for 8 dose |
| DRUG | Misoprostol 800 micrograms | Misoprostol 800 micrograms each 12 hours for 4 doses |
Timeline
- Start date
- 2012-01-01
- Primary completion
- 2012-09-01
- Completion
- 2012-09-01
- First posted
- 2012-01-11
- Last updated
- 2012-10-02
Locations
1 site across 1 country: Iran
Source: ClinicalTrials.gov record NCT01508143. Inclusion in this directory is not an endorsement.