Developing a Complex ex Vivo Endometrial Tissue Model Based on Patient Biopsies to Assess and Optimise the Response to Current and Potential Treatments for Endometriosis

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Endometriosis is a chronic gynaecological disease characterised by the growth of endometrium outside the uterus. It affects 10% of childbearing age women. There is no cure for endometriosis. Hormonal treatments should be the first line therapy. The benefit-risk ratio of symptomatic treatment with hormone therapy varies greatly from one woman to another. The pathophysiology of endometriosis and the mechanisms of action of these treatments are still poorly understood. This may be due to the lack of an optimal experimental model for studying the disease. The aim of this project is to develop a complex ex vivo endometrial model recapitulating the organisation and properties of the human endometrium using innovative tissue bioengineering methods. This model will make it possible to develop a pre-clinical approach that predicts individual response to different types of hormonal treatment in order to optimise therapeutic choices and provide a better understanding of the effects of these treatments.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: f
View:

• Female

• People aged between 18 and 50

• Person who has or has had hormonal contraceptive treatment

• A person who has given written consent

• Person diagnosed with a benign gynaecological pathology not affecting the endometrium and requiring hysterectomy, hysteroscopy or laparoscopy or with a diagnosis of endometriosis and requiring laparoscopy or hysterectomy

• Person affiliated to the french social security

Locations
Other Locations
France
Hôpital Femme Mère Enfant / GHE
RECRUITING
Bron
Hôpital de la Croix-Rousse / GHN
RECRUITING
Lyon
Contact Information
Primary
Charles-André PHILIP, M.D., PhD
charles-andre.philip01@chu-lyon.fr
04 27 85 51 70
Backup
Axelle BRULPORT, PhD
axelle.brulport@inserm.fr
Time Frame
Start Date: 2024-06-21
Estimated Completion Date: 2025-12
Participants
Target number of participants: 45
Treatments
Experimental: Endometriosis
Women with endometriosis who have an indication for gynaecological surgery
Active_comparator: Control
Women with no endometrial pathology who have an indication for gynaecological surgery
Related Therapeutic Areas
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov