Ultrasound Evaluation for Improving Patient Selection in vNOTES

This study is looking at whether a trans-vaginal ultrasound (an ultrasound performed through the vagina) before surgery can help doctors better choose patients for vNOTES (Vaginal Natural Orifice Transluminal Endoscopic Surgery). vNOTES is a type of minimally invasive surgery that avoids large incisions. The study aims to see if using this ultrasound to check for adhesions (scar tissue that can cause organs to stick together) between the uterus and rectum can reduce complications during vNOTES. You may be able to join if you are a woman aged 18 or older, are planning to have a hysterectomy (removal of the uterus) or surgery for an adnexal (ovary or fallopian tube) issue, and are being considered for vNOTES. You cannot join if you have a history of radiation to the pelvis, cancer, or are having other vaginal surgeries at the same time. The study will enroll 75 participants.

Study design
This is an interventional study, meaning participants will receive a specific intervention. It plans to enroll 75 women.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed from recruitment until one month after their operation to measure the rate of adhesions or complicated entry to the Douglas space during surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05623514

Ultrasound Evaluation for Improving Patient Selection in vNOTES

Recruiting
NAAges 18+InterventionalDiagnostic
The University of Texas Health Science Center, Houston
~75 participants
Updated 2024-11-14 on ClinicalTrials.gov
What's tested:Trans-vaginal ultrasound

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
The rate of adhesions/ complicated entry to the Douglas space reported during surgery.
Measured over From recruitment in the clinics until one month post operation
Surgery

NCT05623514

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of Texas

    Houston, Texasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Aya Mohr-Sasson · PRINCIPAL_INVESTIGATOR · The University of Texas Health Science Center, Houston, TX

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Eligibility criteria

Exclusion

History of radiation to the pelvis
Malignancy
Combined current vaginal operation (for the treatment of prolapse/ urinary complaints)
  • The rate of adhesions/ complicated entry to the Douglas space reported during surgery.From recruitment in the clinics until one month post operation