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 @ 1:23 AM
Ignite Modification Date:
2025-12-25 @ 1:23 AM
NCT ID:
NCT01766193
Eligibility Criteria:
Inclusion Criteria:
* first delivery in time period 1990-1997
* vaginal birth, spontaneous, forceps or vacuum extraction, or cesarean section
* residency in Klæbu, Malvik, Melhus, Midtre Gauldal, Rissa, Selbu, Trondheim, Tydal, Åfjord at the time of first delivery
Exclusion Criteria:
* stillbirth
* breech birth
* congenital Abnormalities
* residency outside the 9 selected communities
* forceps delivery following previous vacuum extraction delivery or spontaneous vaginal birth
* vacuum extraction delivery following previous forceps delivery or spontaneous vaginal birth
* Vaginal birth following previous cesarean section
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
40 Years
Maximum Age:
60 Years
Study:
NCT01766193
Study Brief:
Protocol Section:
NCT01766193