RecruitingNot applicableNCT04463316
GROWing Up With Rare GENEtic Syndromes
Studying Prader-Willi syndrome
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
- dr. Laura C. G. de Graaff-Herder
- Intervention
- Retrospective file studies(diagnostic_test)
- Enrollment
- 600 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2018 – 2030
Study locations (1)
- Erasmus Medical Center, Rotterdam, South Holland, Netherlands
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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