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:
2025-12-25 @ 12:17 AM
Ignite Modification Date:
2025-12-25 @ 12:17 AM
NCT ID:
NCT00619658
Eligibility Criteria:
Inclusion Criteria:
* healthy females
* requesting an elective termination of pregnancy by medical abortion
* an intrauterine pregnancy \</= 63 days gestation
* willing and able to sign the informed consent
* willing to comply with the study protocol and visit schedule
* willing to have a surgical abortion/D\&C if indicated
* with easy and ready access to a telephone
Exclusion Criteria:
* contraindication to mifepristone
* contraindication to misoprostol
* cardiovascular disease -hemoglobin \<10 g/dL
* known clotting defect or receiving anticoagulants
* pregnancy with an IUD
* breastfeeding
* ultrasound evidence of an early pregnancy failure
* pelvic examination with evidence of acute cervicitis
* prior participation in this research study
* current participation in a conflicting research study
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00619658
Study Brief:
Protocol Section:
NCT00619658