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 @ 4:50 AM
Ignite Modification Date:
2025-12-25 @ 4:50 AM
NCT ID:
NCT04824118
Eligibility Criteria:
Inclusion Criteria:
Group 1:
* Pregnant and seeking abortion
* Gestation of pregnancy less than 10 weeks
* Healthy, no medical conditions
Group 2:
* Pregnant and seeking abortion
* Gestation of pregnancy between 10 and 14 weeks
* Healthy, no medical conditions
Group 3:
* Pregnant and seeking abortion
* Gestation of pregnancy between 14 to 20 weeks
* Healthy, no medical conditions
Group 4:
* Non pregnant
* Healthy, no medical conditions
* Able to speak English independently
Exclusion Criteria:
All groups:
* Unable to give informed consent
* Previous or current venous thromboembolism
* Current smoker
* Personal or family history of thrombophilia or haemophilia
* Taking medicines known to affect clotting parameters (e.g. Aspirin)
Groups 1-3:
\- Planning to commence hormonal contraception prior to second blood test.
Group 4:
\- Using hormonal contraception at baseline visit
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
16 Years
Study:
NCT04824118
Study Brief:
Protocol Section:
NCT04824118