Impact of Endotest on Quality of Life in Endometriosis Patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort study follows women aged 18 to 43 with an Endotest prescription to explore how the test experience impacts quality of life, emotional well-being, and coping. The study uses a questionnaire-based approach to capture patient-reported outcomes related to diagnostic experience and subsequent care. It leverages sites in France under innovation funding and includes participants who are affiliated with the French healthcare system or have insurance coverage abroad. The device itself combines Next-Generation Sequencing and algorithms to identify endometriosis from saliva and is already in use in several countries. The study focuses on patient-centered outcomes rather than diagnostic performance alone.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Women with a prescription for Endotest
* Women aged 18 to 43
* Who have dated and signed the consent form
* Affiliated with the French healthcare system or covered by health insurance abroad

Exclusion Criteria:

* Contraindications for the use of Endotest:

  1. Current pregnancy;
  2. Medical history of cancer or HIV infection;
  3. Active infection at the time of saliva collection;
* Significant difficulty reading and understanding the language of the country in which the participant is located.

Where it's running

• Clinique Tivoli Ducos
  Bordeaux, Gironde, France Recruiting
• Hôpital privé Saint-Grégoire
  Saint-Grégoire, Ille-et-Vilaine, France Not yet recruiting
• Groupe Hospitalier Bretagne Sud - GHBS - Lorient
  Lorient, Morbihan, France Not yet recruiting
• Hôpital de Mercy - CHR Metz Thionville
  Peltre, Moselle, France Not yet recruiting
• CHU de Saint Etienne
  Saint-Priest-en-Jarez, Pays de la Loire Region, France Not yet recruiting
• Centre Hospitalier de Pau
  Pau, Pyrénées Atlantiques, France Not yet recruiting

Study contacts

• Study coordinator: Fabien Le Floc'h, Project Manager
• Email: fabien.lefloch@monitoring-force.fr
• Phone: +330630447709

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.