Molecular and Cellular Profiling of Uterine Lavage Collected During Gynecologic Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorStanford University
About this trial
This study is a designed as a to test the clinical and technical feasibility of using this novel uterine lavage collection catheter to collected UL samples from up to 50 individuals undergoing gynecologic surgery and to describe the cellular composition of these samples. In order to do this, it is a prospective consecutively-enrolled cohort of 50 participants, all of who will receive the intervention of uterine lavage collection.
Eligibility criteria
Qualifiers
Undergoing gynecologic surgery with Stanford Healthcare
Intact uterus and cervix
At least one intact fallopian tube and ovary (on the same side)
Aged 18 years or older
Disqualifiers
Known endometrial or cervical cancer or endometrial or cervical intraepithelial neoplasia
Status post bilateral salpingectomy or tubal ligation
Lack of consenting capacity
Positive preoperative pregnancy test
Trial design
Treatments tested in this trial
- Uterine Lavage
Treatment groups
50 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov