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 @ 12:13 AM
Ignite Modification Date:
2025-12-25 @ 12:13 AM
NCT ID:
NCT03850158
Eligibility Criteria:
Inclusion Criteria:
* Informed Consent as documented by signature
* Be premenopausal (menopause is defined as amenorrhea lasting one year or longer)
* Patients should be in follicular phase
* Have chronic pelvic pain and/or Infertility and be willing to undergo planned endometriosis resection procedure.
Exclusion Criteria:
* Known or suspected allergy to iodine, shellfish, or ICG dye
* Hyperthyroidism
* Severe renal insufficiency
* Simultaneous therapy with beta-blockers
* Women who are pregnant (positive HCG in the blood) or breast feeding
* Intention to become pregnant during the course of the study
* Inability to follow the procedures of the study (due to language problems, psychological disorders, dementia)
* Active pelvic infection (positive vaginal or cervical smears for bacteria or elevated markers of infection in the blood)
* Previous history of radiation therapy of the pelvis
* Presence of medical conditions contraindicating general anesthesia or standard laparoscopic surgery
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03850158
Study Brief:
Protocol Section:
NCT03850158