Eligibility Module

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 @ 12:12 AM
Ignite Modification Date: 2025-12-25 @ 12:12 AM
NCT ID: NCT06187558
Eligibility Criteria: Inclusion Criteria: * Patients who underwent multiport or single-site-port laparoscopic surgery with at least one transient pelvic organ suspension. * Surgeries performed between March 2019 and May 2021. * Surgeries conducted in the specified tertiary referral hospital. * Patients who provided written informed consent for the surgical procedure and for the use of their personal data in scientific research. * Availability of medical records and videos of surgeries for data collection. * Patients who underwent surgery for one of the following conditions: * Deep infiltrating endometriosis (DIE) * Endometrial Cancer * Pelvic prolapse treated by laparoscopic surgical procedure * Single-port access laparoscopy for benign gynecological diseases * Surgeries performed by either senior surgeon (S.A.) or junior surgeon (M.N.D). Exclusion Criteria: * Surgeries conducted outside the timeframe of March 2019 to May 2021. * Surgeries not involving multiport or single-site-port laparoscopic surgery with pelvic organ suspension. * Patients who did not provide written informed consent. * Absence of medical records or surgery videos for data collection. * Surgeries not performed in the mentioned tertiary referral hospital. * Surgeries not primarily conducted for the specified indications (i.e., DIE, oncological disease, pelvic prolapse). * Surgeries not performed by the listed surgeons (S.A. or M.N.D).
Healthy Volunteers: False
Sex: FEMALE
Study: NCT06187558
Study Brief:
Protocol Section: NCT06187558