Status:
COMPLETED
Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene
Lead Sponsor:
Associação Fundo de Incentivo à Pesquisa
Conditions:
Congenital Central Hypoventilation Syndrome
Eligibility:
MALE
5+ years
Brief Summary
Congenital central hypoventilation syndrome (CCHS) is a rare disorder of respiratory control characterized by ventilatory impairment that results in arterial hypoxemia. Although patients typically pre...
Detailed Description
Congenital central hypoventilation syndrome (CCHS) is a rare disorder of respiratory control characterized by ventilatory impairment that results in arterial hypoxemia. This condition worse during sle...
Eligibility Criteria
Inclusion
- Family member
Exclusion
- NA
Key Trial Info
Start Date :
July 1 2010
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2010
Estimated Enrollment :
1 Patients enrolled
Trial Details
Trial ID
NCT01225679
Start Date
July 1 2010
End Date
September 1 2010
Last Update
February 6 2014
Active Locations (1)
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1
Disciplina de Medicina e Biologia do Sono, Departamento de Psicobiologia, Universidade Federal de São Paulo
São Paulo, São Paulo, Brazil, 04024-002