Clinical Trials Logo

Clinical Trial Summary

This study examined the acceptability and feasibility of introducing a mifepristone-misoprostol regimen of medical abortion into abortion services in two private clinics in Puerto Rico; 2 clinics in Baku, Azerbaijan; 3 clinics in Yerevan, Armenia; and 4 clinics in Mexico City. It was hypothesized that the study regimen would be both acceptable and efficacious.


Clinical Trial Description

The study recruited women with pregnancies up to 63 days gestation. Eligible women took 200 mg mifepristone, followed by 800 buccal misoprostol. They later underwent clinic follow-up to determine if their medical abortions were complete. The study assessed the acceptability and feasibility of the above regimen and sought to determine the efficacy and acceptability of buccal administration of misoprostol as well as the acceptability of side effects experienced by women. ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00386282
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase N/A
Start date September 2006
Completion date March 2011

See also
  Status Clinical Trial Phase
Completed NCT02219100 - Acceptability and Feasibility of a Demedicalized Medical Abortion Regimen in the Caucasus N/A
Completed NCT02398838 - Acceptability and Feasibility of a Simplified Medical Abortion Regimen in Georgia N/A