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PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood

NCT00652964 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2012-11-08

No results posted yet for this study

Summary

Detect the PHOX2B Mutation-confirmed congenital central hypoventilation syndrome

Conditions

  • Central Alveolar Hypoventilation Syndrome

Interventions

DEVICE

CPAP

CPAP treatment for patients with congenital central hypoventilation syndrome

Sponsors & Collaborators

  • National Taiwan University Hospital

    lead OTHER

Principal Investigators

  • Peilin Lee, M.D · National Taiwan University Hospital

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00652964 on ClinicalTrials.gov