MRI vs. Transvaginal Ultrasound in Deep Infiltrating Endometriosis Diagnosis
Data Collection
Collected from past medical records and data - RetrospectiveCohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: June 1, 2025
Actual date on which the first participant was enrolled.This study focuses on improving the diagnosis and surgical planning for women with deep infiltrating endometriosis (DIE), a condition where tissue similar to the lining inside the uterus grows outside it, causing pain and fertility issues. Women of reproductive age are the primary group affected by this condition. Traditionally, diagnosing endometriosis takes several years, partly due to the invasiveness of the gold-standard diagnostic method, laparoscopy. However, non-invasive imaging techniques such as transvaginal ultrasound (TVS) and magnetic resonance imaging (MRI) have shown promise in reducing this delay. This study specifically aims to evaluate how well TVS performs in detecting DIE before surgery and examines whether adding MRI could improve surgical planning. Participants in this study undergo TVS to assess the presence of DIE, with findings being compared to actual surgical observations to measure the accuracy of this imaging technique. The study evaluates how well TVS identifies the location and extent of endometriosis lesions using the #ENZIAN classification system. Additionally, the study investigates if including MRI alongside TVS provides better insights for preoperative planning, especially in complex cases requiring coordination between different surgical specialists. The goal is to determine the best approach to ensure effective treatment and management, ultimately enhancing patient care and outcomes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.200 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location