Mifepristone vs Misoprostol
Recruiting
Phase 1
Interventional Study
Cervical Preparation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Trial phase
- Phase 1
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 94 (estimated)
- Sponsor
- Montefiore Medical Center · Other
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About This Trial
The Investigator team hypothesizes that in a randomized trial comparing mifepristone-alone or misoprostol-alone for cervical preparation for procedural abortions at 12 to 16 weeks in hospital-based care, the proportion of patients who achieve successful cervical dilation will be different between the study groups.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* English or Spanish-speaking
* Capacity to consent
* Seeking induced abortion of a singleton pregnancy between 12 weeks, 0 days and 16 weeks, 6 days (based on age at day of surgery)
Exclusion Criteria:
* History of more than two prior Cesarean deliveries
* Sonographic evidenc…
Contacts