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

U

University Hospital, Rouen

Status

Enrolling

Conditions

Lysosomal Storage Diseases
Neonatal Screening

Treatments

Procedure: Additional blood sampling

Study type

Interventional

Funder types

Other

Identifiers

NCT04393701
2020/007/HP

Details and patient eligibility

About

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).

Enrollment

100,000 estimated patients

Sex

All

Ages

1 to 4 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Newborn in a Normandy maternity hospital
  • Newborn participating in the National Neonatal Screening Program
  • Holder(s) of parental authority having read and understood the information letter and signed the informed consent form

Exclusion criteria

There are no criteria for non-inclusion in this study. Participation in the study, such as participation in the National Neonatal Screening Program, is not mandatory.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100,000 participants in 1 patient group

neonates tested in Normandie, France
Experimental group
Description:
All neonates will be tested in Normandie
Treatment:
Procedure: Additional blood sampling

Trial contacts and locations

0

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Central trial contact

Soumeya BEKRI, Pr; Julien BLOT

Data sourced from clinicaltrials.gov

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