RecruitingNot applicableNCT04463316

GROWing Up With Rare GENEtic Syndromes

Studying Prader-Willi syndrome

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Key facts

Sponsor
dr. Laura C. G. de Graaff-Herder
Intervention
Retrospective file studies(diagnostic_test)
Enrollment
600 enrolled
Eligibility
18 years · All sexes
Timeline
20182030

Study locations (1)

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.

Open NCT04463316 on ClinicalTrials.gov

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