Simplified Medical Abortion Follow-Up
Not Applicable
Terminated
- Conditions
- Pregnancy TestsAbortion
- Registration Number
- NCT02524990
- Lead Sponsor
- Gynuity Health Projects
- Brief Summary
The purpose of this operations research study is to evaluate women's interest in and compliance with using a semiquantitative multi-level dipstick pregnancy test at home for medical abortion follow-up.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Female
- Target Recruitment
- 53
Inclusion Criteria
- She has been determined by the site investigator or designee to be fully eligible for medical abortion with mifepristone followed by misoprostol according to the site's standard criteria;
- She is willing to use the semiquantitative pregnancy test at home;
- She is wiling and able to comply with the study procedures;
- She speaks and reads English;
- She has signed the study informed consent form.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Patients' compliance in performing the semiquantitative pregnancy test and reporting results Within 2 weeks after medical abortion This will be assessed with a survey administered at the scheduled follow-up phone call. The survey will determine if the patient performed the SQPT as requested, and whether they can interpret and report the results correctly.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Carafem Health Center
🇺🇸Chevy Chase, Maryland, United States
Carafem Health Center🇺🇸Chevy Chase, Maryland, United States