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 @ 2:18 AM
Ignite Modification Date:
2025-12-25 @ 2:18 AM
NCT ID:
NCT03412734
Eligibility Criteria:
Inclusion Criteria:
* Undergoing total vaginal, laparoscopic assisted vaginal, total laparoscopic, or robotic-assisted laparoscopic hysterectomy by a physician at Cincinnati Urogynecology Associates or Tri-State Gynecology Oncology TriHealth Inc.
* Concomitant procedures such as vaginal vault suspension, suburethral sling, cystoscopy, enterocele repair, anterior or posterior colporrhaphy, bilateral salpingectomy or salpingooophorectomy, staging procedures, lymph node sampling and other indicated procedures will be included
* English speaking
* Ability to provide consent
Exclusion Criteria:
* Unwillingness to participate in the study
* Non English speaking
* Patients that do not undergo a hysterectomy
* Reported allergy to iodine or chlorhexidine preparation solutions
* Patients undergoing planned debulking surgery for ovarian, fallopian tube or primary peritoneal cancers
* Current infection necessitating hysterectomy
* Active sepsis, pelvic abscess or pelvic inflammatory disease
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03412734
Study Brief:
Protocol Section:
NCT03412734