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Metabolic FingerPrinting (MetaPrint)

A

Arcensus

Status

Enrolling

Conditions

Genetic Disease

Treatments

Other: No intervention

Study type

Observational

Funder types

Industry

Identifiers

NCT05305729
MetaPrint-2021

Details and patient eligibility

About

The MetaPrint study aims to characterize the metabolic fingerprint of genetic diseases in order to enhance knowledge on the physiological disease status and establish so new tools for diagnosing, monitoring and personalizing treatment of genetic diseases.

Enrollment

10,000 estimated patients

Sex

All

Ages

2+ months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Informed consent is obtained from the participant or from the parent/ legal guardian
  • The participant is 2 months or older
  • The participant is diagnosed with a genetic disease
  • The participant is a first degree relative of a subject diagnosed with a genetic disease

Exclusion criteria

  • Informed consent is not obtained from the participant or from the parent/ legal guardian
  • The participant is younger than 2 months
  • The participant is not diagnosed with a genetic disease
  • The participant is not a first degree relative of a subject diagnosed with a genetic disease

Trial design

10,000 participants in 1 patient group

Subjects with a genetic disease
Treatment:
Other: No intervention

Trial contacts and locations

5

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Central trial contact

Volha Skrahina, PhD; Arndt Rolfs, Prof. Dr.

Data sourced from clinicaltrials.gov

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