Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:04 PM
Ignite Modification Date:
2025-12-24 @ 1:04 PM
NCT ID:
NCT05781061
Eligibility Criteria:
Inclusion Criteria:
* Can speak and read English
* Has an address in a state where the study clinicians are licensed to practice medicine and where the service is legal
* Is old enough to consent to abortion and study participation without parental consent in the study state
* Has reviewed the study website
* Has had a positive pregnancy test
* Has signed the study informed consent form (ICF), which will be included within the questionnaire
* Is pregnant with a gestational age of ≤77 days from last menstrual period
* Desires MA
* Has no symptoms of or risk factors for ectopic pregnancy
* Has no medical contraindications to MA, specifically:
Hemorrhagic disorder or concurrent anticoagulant therapy Chronic adrenal failure Concurrent long-term systemic corticosteroid therapy Inherited porphyria Allergy to mifepristone or misoprostol, or other prostaglandin
* Is not asked by the site to have a synchronous consultation with clinician OR facility-based tests such as ultrasound, laboratory tests, examination, etc.
* Is comfortable obtaining the abortion pills without a pre-treatment ultrasound and without speaking by phone or video with the abortion provider.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT05781061
Study Brief:
Protocol Section:
NCT05781061