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Active Not RecruitingNCT06794424

Impact of Ziwig Endotest® on the Management of Patients With Clinical Symptoms of Endometriosis Inconsistent With Their Imaging Work-up

Impact of Ziwig Endotest® on the Decision and Management of Patients With Chronic Disabling Pelvic Pain Strongly Suggestive of Endometriosis and Presenting With a Negative or Uncertain Baseline Imaging Workup

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
2,503 (actual)
Sponsor
ZIWIG · Industry
Sex
Female
Age
18 Years – 43 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to evaluate the impact of Ziiwg Endotest on patient management decisions before and after the test. The main questions it aims to answer are: * Does the test reduce the intention and number of laparoscopies in women whose decision to undergo laparoscopy was made before the test result was obtained? * Does the test change management decisions in women with no prior indication for diagnostic laparoscopy? Study will compare the patient management decision before and after the test. The acts and procedures performed as part of this research are : * Aa saliva sampling (Ziwig Endotest) at inclusion * A mutidisciplinary meeting post test (if applicable) * Completion at inclusion and 6 month of a quality-of-life questionnaire (EHP-5) * Completion at inclusion and 6 month of a VAS for pain * Completion at inclusion and 6 month of a Likert satisfaction scale * A test results Announcement consultation * A visit at 6 months.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTZiwig Endotest®Saliva sampling for Endometriosis diagnostic

Timeline

Start date
2025-03-14
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2025-01-27
Last updated
2026-03-25

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06794424. Inclusion in this directory is not an endorsement.

Impact of Ziwig Endotest® on the Management of Patients With Clinical Symptoms of Endometriosis Inconsistent With Their (NCT06794424) · Clinical Trials Directory