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 @ 5:31 PM
Ignite Modification Date:
2025-12-24 @ 5:31 PM
NCT ID:
NCT02811068
Eligibility Criteria:
Inclusion Criteria:
* Participant is willing and able to give written informed consent for participation.
* Females originally enrolled in the randomised parallel group study
Exclusion Criteria:
* Known bleeding diathesis (or any condition that may be associated with a prolonged bleeding time).
* Any other significant condition or circumstance which, in the opinion of the investigator, may either put the participant at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT02811068
Study Brief:
Protocol Section:
NCT02811068