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Clinical Trials in Belgium / NCT06994091
Starting soon Observational

Imaging Comparison for the Preoperative Planning and Diagnosis of DIE: a Multicenter Retrospective Study.

NCT06994091 · tracked via the Priya Life Science Belgium tracker
Phase
Observational
Started
2025-06-01
Last updated
2025-05-29

Condition(s) studied

Deep EndometriosisSurgeryTransvaginal UltrasoundMRIPreoperative Planning

Study summary

Several centers in Belgium use both transvaginal ultrasound (TVS) and magnetic resonance imaging (MRI) for the preoperative diagnosis of deep infiltrating endometriosis (DIE), while other centers rely almost exclusively on TVS. From the perspective of both the patient and the endometriosis care team, it is not primarily important that every individual lesion is mapped perfectly preoperatively, but rather that all lesions impacting clinical management and surgical planning are accurately detected. This is particularly crucial when a multidisciplinary approach is required, involving a urologist for bladder lesions and/or an abdominal surgeon for invasive rectosigmoid lesions. Moreover, providing the patient with thorough preoperative counseling is essential, and this is, of course, determined by the preoperative findings and the type of planned surgical procedure.

In this study, we first assess the diagnostic performance of TVS in the preoperative diagnosis of DIE. As a secondary objective, we evaluate the added value of MRI compared to TVS for preoperative surgical planning in patients who also underwent an MRI examination.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * All patients who underwent preoperative imaging at AZ Sint-Jan AV and Ziekenhuis Oost-Limburg (ZOL) between October 2021 and December 2024, TVS with or without complementary MR followed by therapeutic surgery as part of DIE. Exclusion Criteria: * Performing imaging, TVS with or without additional MR, by an operator without specific experience in the field. * Lack of a TVS report diagnosing DIE. * Preoperative diagnosis of only superficial endometriosis and/or endometriomas without DIE. * Performance of surgery by a surgeon without specific experience in the field. * Lack of a surgical report that correctly describes all DIE lesions.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ziekenhuis Oost-Limburg Genk Limburg

More Ziekenhuis Oost-Limburg trials in Belgium

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06994091 on ClinicalTrials.gov ↗ ← All trials in Belgium