Menstrual Regulation Clinical Trial
Official title:
Introducing Mifepristone-Misoprostol for Menstrual Regulation in Public Sector Facilities in Bangladesh
This open-label study is being conducted to determine whether a mifepristone-misoprostol regimen for uterine evacuation which consists of 200 mg mifepristone followed 24 hours later by 800 mcg buccal misoprostol is acceptable to women and providers and feasible for introduction in public sector facilities in Bangladesh. It will also determine the feasibility of women availing the option of taking their dose of misoprostol outside the facility.
This open-label study is being conducted to determine whether a mifepristone-misoprostol
regimen for uterine evacuation which consists of 200 mg mifepristone followed 24 hours later
by 800 mcg buccal misoprostol is acceptable to women and providers and feasible for
introduction in public sector facilities in Bangladesh. It will also determine the
feasibility of women availing the option of taking their dose of misoprostol outside the
facility.
The specific aims of this project are as follows:
- Assess whether a uterine evacuation regimen that allows women the option of taking
their misoprostol outside the facility and which consists of 200 mg mifepristone
followed 24 hours later by 800 mcg buccal misoprostol is feasible for introduction in a
range of clinical settings in government facilities in Bangladesh;
- Determine whether a mifepristone-misoprostol regimen for uterine evacuation is
acceptable to women and providers; and
- Determine what proportion of women, if offered the choice, would prefer to take
misoprostol in the facility and what proportion would prefer to take it outside the
facility.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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