CompletedNCT01225679
Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene
Studying Congenital central hypoventilation syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Associação Fundo de Incentivo à Pesquisa
- Principal Investigator
- Lia Rita A Bittencourt, PhDUniversidade Federal de São Paulo/UNIFESP
- Intervention
- positive airway pressure, Non-invasive mechanic ventilation(device)
- Enrollment
- 1 enrolled
- Eligibility
- 5 years · MALE
- Timeline
- 2010 – 2010
Study locations (1)
- Disciplina de Medicina e Biologia do Sono, Departamento de Psicobiologia, Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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