Craniofacial Microsomia: Accelerating Understanding of the Significance and Etiology
Completed
Conditions studied: Microtia, Microtia-Anotia, Craniofacial Microsomia, Goldenhar Syndrome, OAVS, OAV Syndrome, Hemifacial Microsomia
In brief
The CAUSE study is a multicenter study, with domestic (n=4) and international (n=6) study sites. Children and young adults (ages 0-18) who have microtia and/or craniofacial microsomia and their parents are invited to participate. Children and parents are asked to provide a DNA sample (blood or saliva) and are asked to upload a few photos of their face. Parents are asked a short interview. Participants are able to participate from home or at one of four domestic sites.
Key facts
- Study ID
- NCT04351893
- Run by
- Seattle Children's Hospital
- People needed
- 935
- Starts
- 2018-02-23
- Expected to finish
- 2023-08-30
- Last updated by the study team
- 2024-04-22
Who can join
Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Children's Hospital Los Angeles — Los Angeles, California, United States
- University of North Carolina — Chapel Hill, North Carolina, United States
- Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States
- Seattle Children's Hospital — Seattle, Washington, United States
- Pontificia Universidad Javeriana — Bogotá, Colombia
- ICESI — Cali, Colombia
- Pontificia Universidad Javeriana — Cali, Colombia
- Clínica Comfamiliar Risaralda — Pereira, Colombia
- Hospital Edgardo Rebagliati Martins — Lima, Peru
- Instituto de Genética Médica y Molecular (INGEMM) — Madrid, Spain
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.