Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia (ECP-012)

NCT ID: NCT01629927

Last Updated: 2012-06-28

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2012-03-31
• Study Completion Date: 2012-06-30

Brief Summary

The study proposes to enroll male subjects affected by Hypohidrotic Ectodermal Dysplasia (XLHED). The sweat duct images will be acquired with a CE marked skin-imaging device and the sweat rate will be measured using a CE marked pilocarpine iontophoresis and collection system. The technologies for both imaging of sweat ducts and the measurement of maximal sweat rate have been used safely and without adverse events in our prior studies involving HED/XLHED subjects. Furthermore, this study will assess the feasibility of developing a non-invasive screening tool that will enable detection of clinical signs of XLHED based on an analysis of a two dimensional frontal photograph.

Detailed Description

The study proposes to enroll male subjects affected by XLHED (determined by genetic testing and restricted to age > 1 yr). The sweat duct images will be acquired with a CE marked skin-imaging device and the sweat rate will be measured using a CE marked pilocarpine iontophoresis and collection system. The technologies for both imaging of sweat ducts and the measurement of maximal sweat rate have been used safely and without adverse events in our prior studies involving HED/XLHED subjects. Furthermore, this study will assess the feasibility of developing a non-invasive screening tool that will enable detection of clinical signs of XLHED based on an analysis of a two dimensional frontal photograph.

Conditions

X-linked Hypohidrotic Ectodermal Dysplasia; Hypohidrotic Ectodermal Dysplasia

Study Groups

HED-affected males

Male subjects affected by HED

No interventions assigned to this group

Male controls

Male subjects not affected by HED

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

Subjects must meet all of the following criteria to be enrolled in this study.

• Attending the 2012 Spanish Association for those Affected by Ectodermal Dysplasia Annual Reunion;
• One year of age or greater;
• Conform to one of the following requirements for providing informed consent/assent:

• If more than 18 years of age, subjects must provide signed informed consent;
• If less than 18 years of age and it is determined that the subject is capable of providing assent, both the assent of the subject and consent of the parent(s) or guardian of that subject must be granted. Under this condition, both parents of the subject should give their permission, unless 1 parent is deceased, unknown, incompetent, or not available;
• If the subject is incapable of providing assent, the consent of the parent(s) or guardian of the subject must be granted. Under this condition, both parents should give their consent, unless 1 parent is deceased, unknown, incompetent, or not available.
• Can provide documentation of genetic testing results positive for an EDA gene mutation /deletion;
• As described in Section 3.2 above, subjects must meet one of the following criteria:

• Documented diagnosis of XLHED confirmed via genetic testing;
• Unaffected male controls.

Exclusion Criteria

• Known hypersensitivity to pilocarpine or pilocarpine-like muscarinic agonists;
• Presence of pacemakers;
• Subjects who are not able or are not willing to comply with the procedures of this protocol;
• Subjects with any major medical problem that will prevent them from participating in this study.

• Minimum Eligible Age: 1 Year
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Edimer Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Encarna Navarro, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Hospital Universitario Virgen de la Arrixaca

Locations

Center for Rare Diseases

Burgos, , Spain

Countries

Spain

Other Identifiers

ECP-012

Identifier Type: -

Identifier Source: org_study_id