RCDP - Rhizomelic Chondrodysplasia PunctataRare diseaseChildren's health
What this study is
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.
Study details
- Official title
- Rhizomelic Chondrodysplasia Punctata Registry at Nemours Children's Health
- Sponsor
- Nemours Children's Clinic
- Conditions
- RCDP - Rhizomelic Chondrodysplasia Punctata · RCDP1 · RCDP2 · RCDP3 · RCDP4 · RCDP5
- Enrolling
- 100 people
- Starts
- 2013-05-17
- Est. completion
- 2030-01-01
- Record
- View on ClinicalTrials.gov ↗
Who can join
Sex ALLHealthy volunteers Not acceptedYou may qualify if
- Diagnosed with RCDP or closely related conditions by metabolic and/or genetic testing
You can't join if
- Not meeting diagnosis of RCDP or closely related conditions by study team physician review of prior metabolic and/or genetic testing
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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1
Study locations (1)
1 openNemours
Wilmington, Delaware, United States
- Emily Longenecker, BS · Contact302-298-7978emily.longenecker@nemours.org
- Mahim Jain, MD, PhD · Principal investigator
Recruiting
Study team
Sponsor
Nemours Children's Clinic
Study ID MB002
Principal investigator
Mahim Jain, MD, PhD
Nemours
Have questions? The contacts above can answer them before you apply.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.