Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Seattle Children's Hospital
With
National Institute of Dental and Craniofacial Research (NIDCR)
Children's Hospital Los Angeles
Children's Hospital of Philadelphia
University of North Carolina
Northwestern University
University of Illinois Chicago
University of Washington
University of Pittsburgh
New York University
Age
1–2
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
We are currently looking to enroll children with craniofacial microsomia through ClinicalTrials.gov
Children with Craniofacial Microsomia:
1. Male or female infant participant is between 12 months and 24 months of age, or corrected age (for some infants born prior to their due date).
2. Infant participant has diagnosis of at least one of the following conditions:
* Microtia
* Anotia
* Facial asymmetry AND Preauricular tag(s)
* Facial asymmetry AND Facial tag(s)
* Facial asymmetry AND Epibulbar dermoid
* Facial asymmetry AND Macrostomia (i.e., lateral cleft)
* Preauricular tag AND Epibulbar dermoid
* Preauricular tag AND Macrostomia
* Facial tag AND Epibulbar dermoid
* Macrostomia AND Epibulbar dermoid
3. Infant participant has been diagnosed by a regional craniofacial team.
4. Legal guardian will provide written parental permission and informed consent prior to participation in study.
5. Legal guardian is willing to comply with all study procedures and be available for the duration of the study through Time 3.
Parents of Children with Craniofacial Microsomia:
able to provide written consent for study participation,
willing to comply with all study procedures and
interested in participating in the entire study through Time 3.
You may not be if
Children with Craniofacial Microsomia:
1. Subject is diagnosed with a known syndrome that involves microtia and/or underdevelopment of the jaw (Townes-Brocks, Treacher Collins, branchiootorenal, Nager, or Miller syndromes).
2. Subject has abnormal chromosome studies (karyotype)
3. Subject has a major medical or neurological condition that prevents participation in the study (e.g., cancer, cerebral palsy) at time of recruitment
4. Subject was born before 34 weeks estimated gestational age
5. Anything that would place the subject at increased risk or preclude the subject's full compliance with or completion of the study.
6. Sibling already participating in the CLOCK study
7. Subject's consenting parent does not speak English or Spanish
Parents of Children with Craniofacial Microsomia
1. Anything that would preclude the subject's full compliance with or completion of the study.
2. Subject does not speak English or Spanish
Clareo Health | Craniofacial Microsomia: Longitudinal Outcomes in Children Pre-Kindergarten (CLOCK)
