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Clinical Trial Summary

The objective of this study is to understand the mechanisms of rejection in uterine transplantation and to search for non-invasive markers of rejection. The biological samples necessary for our research have been or will be collected during procedures (biopsies, smears, vaginal swab, blood tests) carried out as part of the scheduled follow-up of patients. These will be samples whose collection is minimally or not invasive


Clinical Trial Description

In the context of uterine transplantation, non-invasive rejection markers will be sought by different approaches, including transcriptomics on a prospective cohort of patients with different types of samples: blood, smear and biopsy. A microbiota study will also be carried out. 3 groups will be studied: 1 group of 10 patients benefiting or having benefited from a uterine transplant, 1 second group made up of their 10 donors, 1 group of 10 control women ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04615221
Study type Interventional
Source Hopital Foch
Contact Marie Carbonnel, MD
Phone +331 46 25 48 53
Email m.carbonnel@hopital-foch.com
Status Recruiting
Phase N/A
Start date September 21, 2020
Completion date September 2028

See also
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Completed NCT01338779 - Study of Tolerant Kidney Transplant Recipients N/A
Recruiting NCT05156710 - BIVV020 (SAR445088) n Prevention and Treatment of Antibody-mediated Rejection (AMR) Phase 2
Completed NCT03582436 - Rejection Diagnosis in Kidney Transplants Patients
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Completed NCT01236378 - Study To Evaluate Pharmacokinetics Of Sirolimus In Stable Renal Transplant Recipients Phase 1