Natural History and Outcomes in X-Linked Hypohidrotic Ectodermal Dysplasia
NCT ID: NCT02099552
Last Updated: 2017-09-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
150 participants
OBSERVATIONAL
2014-04-30
2016-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
OTHER
Study Groups
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XLHED
Those with the condition of XLHED
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
1. Confirmed genetic diagnosis of XLHED
2. Written informed consent of both parents (if reasonably available)
Exclusion Criteria
1. Medically-significant complications or congenital anomalies outside of those considered to be associated with the diagnosis or status of XLHED
2. Having received an investigational study drug prior to enrollment. For subjects less than 6 months of age, the mother cannot have taken an investigational drug during her pregnancy.
3. Known hypersensitivity to pilocarpine or pilocarpine-like muscarinic agonists
4. Presence of pacemakers
36 Months
ALL
No
Sponsors
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Edimer Pharmaceuticals
INDUSTRY
Responsible Party
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Principal Investigators
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Ramsey Johnson, MSM
Role: STUDY_DIRECTOR
Edimer Pharmaceuticals
Locations
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University of California, San Francisco
San Francisco, California, United States
Children's National Medical Center
Washington D.C., District of Columbia, United States
Washington University School of Medicine
St Louis, Missouri, United States
Hôpital Necker-Enfants Malades
Paris, , France
University Hospital Erlangen
Erlangen, Bavaria, Germany
Azienda Ospedaliera-Polo Universitario "Luigi Sacco"
Milan, , Italy
University Hospital of Wales
Cardiff, , United Kingdom
Countries
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Other Identifiers
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ECP-015
Identifier Type: -
Identifier Source: org_study_id
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