X Linked Hypohidrotic Ectodermal Dysplasia Clinical Trial
— ECP-014Official title:
Phenotypic Properties in Individuals Affected With X-linked Hypohidrotic Ectodermal Dysplasia: Symptoms and Facial Recognition
Verified date | November 2013 |
Source | Edimer Pharmaceuticals |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Observational |
The current study design incorporates two previously developed, non-invasive approaches to characterize the phenotype of individuals affected with XLHED.
Status | Completed |
Enrollment | 30 |
Est. completion date | September 2013 |
Est. primary completion date | July 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 4 Years and older |
Eligibility |
Inclusion Criteria: 1. Females of original gender of age 18-45 years who are registered and attending the 2013 NFED Family Conference. This will include those at risk for XLHED and controls 2. XLHED-affected males of original gender of age 4 yrs and up who are registered and attending the 2013 NFED Family Conference 3. Provide informed consent/assent Exclusion Criteria: 1. Subjects who are not able or are not willing to comply with the procedures of this protocol 2. Subjects with any major medical problem that will prevent them from participating in this study 3. Male subjects who participated in the prior study ECP-003 sponsored by Edimer Pharmaceuticals Inc. in May 2011 in San Francisco, CA 4. Males at risk for XLHED with prior genetic testing that did not reveal an EDA mutation |
N/A
Country | Name | City | State |
---|---|---|---|
United States | Omni Houston Hotel | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
Edimer Pharmaceuticals |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To collect demographic and clinical status information in XLHED-affected males, adult females at risk for XLHED and adult female controls | To collect demographic and clinical status information in XLHED-affected males, adult females at risk for XLHED and adult female controls using a medical questionnaire | Study day 1 | No |
Primary | To test and refine a computer algorithm for facial recognition of XLHED | To test and refine a computer algorithm for facial recognition of XLHED based on 2D facial photographs obtained from subjects at risk for XLHED and controls | Study day 1 | No |
Primary | To evaluate 3-dimensional facial imaging technology for mapping craniofacial development in XLHED males | To evaluate 3-dimensional facial imaging technology for mapping craniofacial development in XLHED males | Study day 1 | No |
Primary | To test for the presence of genetic mutations in subjects at risk for XLHED | To test for the presence of genetic mutations in subjects at risk for XLHED who lack prior genetic diagnosis | Study day 1 | No |
Primary | To test the validity of a using saliva samples for genetic testing | To test the validity of a using saliva samples for genetic testing buy simultaneously perform genetic testing on blood and salvia and comparing the mutations identified | Study day 1 | No |