Clinical Trial

Proteomic Analysis of Amniotic Fluid to Predict Postnatal Renal Function in Fetuses With Renal and Urinary Tract Malformations

Study acronym: PAPER FACE
Recruiting
View on ClinicalTrials.gov →
Summary
The aim of this project is to validate a previously established amniotic fluid 98 peptide signature predictive of post-natal outcome in fetuses with congenital anomalies of the kidney and the urinary tract (CAKUT) in a "real" clinical context. It includes the feasibility of collecting, transporting and analyzing the amniotic fluid peptidome from clinical centers all over France and of providing the result in a clinically accepted time-frame. Therefore, this multicenter study will not only allow to determine the added value of such new prenatal test but also to ensure the feasibility of its introduction in the management of CAKUT pregnancies.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-03-31.
Status change: Not Yet Recruiting → Recruiting 2026-04-28
Trial Details
NCT Number NCT06912490
Lead Sponsor University Hospital, Toulouse
Conditions Kidney Diseases
Enrollment 78 participants
Start Date 2025-07-18
Primary Completion 2029-12-20 (estimated)
Study Completion 2029-12-20 (estimated)
Updated on ClinicalTrials.gov 2026-05-04