Rhizomelic Chondrodysplasia Punctata Registry
Recruiting now
Conditions studied: RCDP - Rhizomelic Chondrodysplasia Punctata, RCDP1, RCDP2, RCDP3, RCDP4, RCDP5
In brief
The goal of this registry is to collect medical information on individuals with rhizomelic chondrodysplasia punctata and closely related conditions. The study team hopes to learn more about these conditions and improve the care of people with it by establishing this registry.
Key facts
- Study ID
- NCT04569162
- Run by
- Nemours Children's Clinic
- People needed
- 100
- Starts
- 2013-05-17
- Expected to finish
- 2030-01-01
- Last updated by the study team
- 2026-08-07
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with RCDP or closely related conditions by metabolic and/or genetic testing
You may not qualify if…
- Not meeting diagnosis of RCDP or closely related conditions by study team physician review of prior metabolic and/or genetic testing
Where it is running
- Nemours — Wilmington, Delaware, United States (enrolling)
Full record on ClinicalTrials.gov
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