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RECRUITING
NCT04393701
NA

A Pilot Study for Systematic Neonatal Screening for Lysosomal Storage Diseases Using Tandem Mass Spectrometry

Sponsor: University Hospital, Rouen

View on ClinicalTrials.gov

Summary

The study will include all newborns in Normandie region for 3 years (about 105,000 births) for whom signed consent by one (or two) parents will be collected. Based on our previous pilot study (2011) assessing MCAD and PKU using tandem mass spectrometry-based method in Normandie region in which informed consents have been signed for all newborns (43,000) but we are expecting a great willingness to participate to this project. Thus, we are aiming to include 100,000 newborns, and the study will be continued until we reach at least this target. The primary objective is to evaluate the epidemiology of MPS1 and Pompe disease using dried blood samples in the first cohort of neonates tested in France (Normandie region).

Key Details

Gender

All

Age Range

1 Day - 4 Days

Study Type

INTERVENTIONAL

Enrollment

100000

Start Date

2021-03-08

Completion Date

2026-12-08

Last Updated

2025-09-11

Healthy Volunteers

No

Interventions

PROCEDURE

Additional blood sampling

Additional blood sampling on blotting paper will be done in neonates in Normandy, France, compared to National neonatal screening program

Locations (2)

Caen University Hospital

Caen, France

Rouen University Hospital

Rouen, France