Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected by Hypohidrotic Ectodermal Dysplasia - A
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ClinicalTrials.gov Identifier: NCT01293565 |
Recruitment Status :
Completed
First Posted : February 10, 2011
Last Update Posted : June 28, 2012
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Condition or disease |
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Hypohidrotic Ectodermal Dysplasia |
Study Type : | Observational |
Actual Enrollment : | 27 participants |
Official Title: | Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected by Hypohidrotic Ectodermal Dysplasia |
Study Start Date : | February 2011 |
Actual Primary Completion Date : | May 2011 |
Actual Study Completion Date : | July 2011 |

Group/Cohort |
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HED Affected Males |
Male Controls |
- To assess the hair follicle density and percent anagen hairs in the scalp of HED/XLHED males and unaffected controls [ Time Frame: Day 1 and Day 3-4 ]
- To assess the palmar sweat duct number using confocal microscopy in HED/XLHED males and unaffected controls [ Time Frame: Day 1 ]
- To evaluate 3-dimensional imaging technology without radiation exposure for mapping craniofacial development in HED/XLHED males and unaffected controls [ Time Frame: Day 1 ]
- To use teeth impressions to construct 3-dimensional dental models for detailed evaluation of abnormalities present in HED/XLHED males (not for controls) [ Time Frame: Day 1 ]
- To determine the presence or absence of EDA gene mutations/deletions in males with a clinical diagnosis of HED (not for controls) [ Time Frame: Day 1 ]
- To assess by medical history the prevalence of medical complications in HED/XLHED males and unaffected controls [ Time Frame: Day 1 ]
- To assess the pilocarpine-stimulated sweat rate on the volar surface of the forearm following pilocarpine iontophoresis in HED/XLHED males and unaffected controls, and to correlate with heat-stimulated sweat test classification [ Time Frame: Day 1 ]
Biospecimen Retention: Samples With DNA

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Ages Eligible for Study: | 14 Years to 29 Years (Child, Adult) |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Males age 14-29 years with clinical diagnosis of HED
- No scalp shaving in the 6 months prior to enrollment
- No current medical therapy for hair loss
- Written informed consent for study and genotyping (or signed medical release of previous genetic test results)
Exclusion Criteria:
- Medically significant condition as determined by the PI
- Known hypersensitivity to pilocarpine or pilocarpine-like muscarinic agonists (e.g. Urecholine, Salagen, Pilocar, Provocholine)
- Presence of cardiac pacemaker

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01293565
United States, California | |
University of California | |
San Francisco, California, United States, 94143 |
Principal Investigator: | Ophir Klein, MD, PhD | University of California, San Francisco |
Responsible Party: | Edimer Pharmaceuticals |
ClinicalTrials.gov Identifier: | NCT01293565 |
Other Study ID Numbers: |
ECP-003 |
First Posted: | February 10, 2011 Key Record Dates |
Last Update Posted: | June 28, 2012 |
Last Verified: | June 2012 |
X-Linked Hypohidrotic Ectodermal Dysplasia Hypohidrotic Ectodermal Dysplasia XLHED HED |
Ectodermal Dysplasia Ectodermal Dysplasia 1, Anhidrotic Hyperplasia Pathologic Processes Abnormalities, Multiple Congenital Abnormalities |
Skin Abnormalities Skin Diseases, Genetic Genetic Diseases, Inborn Skin Diseases Genetic Diseases, X-Linked |