RecruitingNot applicableNCT05843851
Genetic Newborn Screening for Cystinosis and Primary Hyperoxaluria
Studying Cystinosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Cystinose Stiftung
- Principal Investigator
- Sonja FroschauerCystinosis Foundation (Cystinose Stiftung)
- Intervention
- Diagnostic test(diagnostic_test)
- Enrollment
- 200000 enrolled
- Eligibility
- All sexes
- Timeline
- 2022 – 2026
Study locations (1)
- Screening Laboratory Hanover, Hanover, Lower Saxony, Germany
Collaborators
Screening Laboratory Hannover · Pediatry Kastanienhof Koeln · Medical Genetics Mainz · University Hospital Cologne
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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