Intraoperative Ultrasound in Bowel Deep Endometriosis
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorFundacion Dexeus
About this trial
This study investigates the use of intraoperative transvaginal (IOTVUS) and/or endorectal ultrasound (IOERUS) in the surgical treatment of bowel deep infiltrating endometriosis (DIE).
Eligibility criteria
Qualifiers
Preoperative sonographic and/or MRI findings suggestive of bowel DIE (uterosacral ligaments, posterior vaginal wall, parametrium, retrocervical area, rectovaginal septum, rectum, and/or sigmoid colon).
Scheduled for surgical treatment (laparoscopy or robot-assisted laparoscopy).
Planned postoperative follow-up for at least 12 months.
Written informed consent provided before surgery.
Disqualifiers
Planned surgery for diagnostic purposes only.
Pregnancy at the time of enrollment.
Poor understanding of Spanish or English.
Trial design
Treatments tested in this trial
- intraoperative ultrasound for the assessment of bowel deep infiltrating endometriosis
Treatment groups
200 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov