Intraoperative Intraabdominal Ultrasound for Endometriosis

Sponsor
University of Palermo (Other)
Overall Status
Recruiting
CT.gov ID
NCT05812937
Collaborator
(none)
70
1
23
3

Study Details

Study Description

Brief Summary

The diagnosis of bowel endometriosis lesions is in most cases a combination of anamnesis, clinical exam, transvaginal ultrasound (and/or MRI and/or endorectal sonography) and laparoscopy.

Both the transvaginal ultrasound as well as the MRI have showed a great accuracy with very good sensititivity and specificity regarding the imaging diagnosis of bowel endometriosis.

The conventional laparoscopy contributes to the diagnosis of bowel endometriosis by visualizing the nodules and palpating the deep endometriosis nodule using the instruments, therefor offering the surgeon a haptic feedback by grasping, pushing and rolling the bowel wall and the nodules. Horace Roman and Dan Martin showed that 25% of patients undergoing a conventional laparoscopic segmental bowel resection with a minilaparotomy hat palpable non-visualized endometriosis nodules. These nodules could be directly palpated with the hands because the bowel was exteriorized through the minilaparotomy. The direct palpation of the bowel offers of course a superior haptic feedback compared to the haptic feedback offered by the laparoscopic palpation using the instruments. However this was a direct palpation of only the oral part of the bowel. The aboral part of the bowel caudal to the staple line could not be evaluated by direct palpation. New surgical techniques for the segmental bowel resection with transvaginal/transanal NOSE(natural orifice specimen extraction) have been described in the last years. The novel techniques avoid the minilaparotomy and assure a 100% minimal invasive approach offering better esthetic outcomes.

However in such cases a direct palpation of the bowel wall using the hands in order to identify non- visualizable nodules is not possible as the bowel remains the whole time of the procedure inside of the abdomen. On the other side the robotic-assisted laparoscopy doesn't offer the surgeon a haptic feedback at all. In these cases the surgeon has to rely on the visual aspects of the lesions and therefor "touch" the lesions with his eyes - the visual information should replace the haptic feedback. So in the case of a robotic assisted laparoscopic segemental bowel resection with a NOSE it is not possible to palpate the bowel at all - neither with instruments, not with the hands. Other surgical techniques used to excise smaller colorectal nodules are the rectal shaving and the full thickness excision (disc excision) using a circular stapler. In these situations the surgeon has to rely exclusively on the visual information as well on the haptic feedback given by the conventional laparoscopic instruments. In more than 30% of the cases of full thickness rectal resection the resection the margins are infiltrated by the endometriosis nodules. All the above mentioned situations raise the question of the radicallity in terms of healthy resection margins and of multifocal lesions that cannot be visualized and/or palpated. In this study we are evaluating the diagnostic value of the intraoperative intraabdominal ultrasound for deep infiltrating colorectal endometriosis.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intraabdominal ultrasound

Study Design

Study Type:
Observational
Anticipated Enrollment :
70 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Diagnostic Value of the Intraoperative Intraabdominal Ultrasound for Deep Bowel Endometriosis
Actual Study Start Date :
Jan 1, 2022
Actual Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Women with suspicion of deep bowel endometriosis

Women with suspicion of deep bowel endometriosis undergoing intraoperative ultrasound to assess its diagnostic value for endometriosis patients as well as the predictive potential of changing the therapeutic strategy during the surgery based on the ultrasound findings.

Procedure: Intraabdominal ultrasound
To assess the diagnostic value of the intraoperative intrabaabdominal ultrasound (IIUS) for endometriosis patients as well as the predictive potential of changing the therapeutic strategy during the surgery based on the ultrasound findings.
Other Names:
  • Laparoscopic visualization
  • Laparoscopic palpation
  • Direct palpation in case of a conventional segmental bowel resection with specimen extraction per minilaparotomy.
  • Outcome Measures

    Primary Outcome Measures

    1. Accuracy of IIUS compared to TVS regarding the colorectal endometriosis [At the moment of the surgery]

      Compare the dimmensions of preop. TVS-diagnosed nodules with the intraop. IUS dimensions.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All the patients with suspicion of endometriosis who undergo surgery.
    Exclusion Criteria:
    • Patients under 18 years old;

    • Patients who didn't sign the informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Albertinen Hospital Hamburg Germany 22457

    Sponsors and Collaborators

    • University of Palermo

    Investigators

    • Principal Investigator: Alin Constantin, M.D., Albertinen Hospital Hamburg
    • Study Director: Antonio Simone Laganà, M.D. Ph.D., University of Palermo
    • Study Chair: Andrea Etrusco, M.D., University of Palermo
    • Study Chair: Vito Chiantera, M.D. Ph.D., University of Palermo

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Andrea Etrusco, M.D., University of Palermo
    ClinicalTrials.gov Identifier:
    NCT05812937
    Other Study ID Numbers:
    • INTA-US-ENDO
    First Posted:
    Apr 14, 2023
    Last Update Posted:
    Apr 14, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Andrea Etrusco, M.D., University of Palermo
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 14, 2023