Actively Recruiting
Molecular and Cellular Profiling of Uterine Lavage Collected During Gynecologic Surgery
Led by Stanford University · Updated on 2025-11-05
50
Participants Needed
1
Research Sites
62 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Molecular and Cellular Profiling of Uterine Lavage Collected During Gynecologic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
- Ability to understand and willing to provide written informed consent
You will not qualify if you...
- Known endometrial or cervical cancer or endometrial or cervical intraepithelial neoplasia
- History of bilateral salpingectomy or tubal ligation
- Lack of capacity to consent
- Positive pregnancy test before surgery
- Active uterine bleeding such as menstruation
- Presence of an intrauterine device (IUD)
- Non-English speaking requiring an interpreter
AI-Screening
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Trial Site Locations
Total: 1 location
1
Stanford University
Palo Alto, California, United States, 94304
Actively Recruiting
Research Team
R
Rozelle Laquindanum
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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