Viewing Study NCT05815134


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Ignite Modification Date: 2025-12-28 @ 12:12 AM
Study NCT ID: NCT05815134
Status: COMPLETED
Last Update Posted: 2025-11-25
First Post: 2023-03-20
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Cell Free DNA Quantification in Patients With Endometriosis Followed Witd Medical Assistance to Procreation
Sponsor: Centre Hospitalier Universitaire, Amiens
Organization:

Study Overview

Official Title: Cell Free DNA Quantification in Patients With Endometriosis Followed Witd Medical Assistance to Procreation
Status: COMPLETED
Status Verified Date: 2025-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ENDO-FIV
Brief Summary: Endometriosis is a common benign disease in premenopausal women and causes chronic pelvic pain and infertility. This infertility may be due to pelvic adhesions and surgery but also because of poor oocyte quality. It is known that endometriosis is associated with an increase oxidative stress, wich induce chronic inflammation, deleterious effect for DNA, proteins and can caused cellular death. ROS markers found in follicular fluid or in serum are significatively higher in endometriosis women. The investigators want to dose a marker of apoptosis in infertile women and see if it's significatively higher in serum and in follicular fluid of patients with endometriosis compared to others infertility causes and if it's correlated to oocyte quality and IVF results. Real time PCR will be used to dose cell free DNA in serum and follicular fluid of patients undergoing IVF treatment (endometriosis and infertility due to tubal factor, male infertility or idiopathic cause). Then the investigators will compare cell free DNA rate with oocyte and embryo quality and with pregnancy outcomes in the different group.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: