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Sleep in Patients With Cystic Fibrosis

NCT00804661 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 76

Last updated 2010-06-03

No results posted yet for this study

Summary

The aim of the study is to identify the parameters that are associated with nocturnal hypoventilation in children and adults with cystic fibrosis. Included patients will undergo a nocturnal evaluation of their gas exchange and sleep quality by actigraphy during their annual check up. The aim is thus to identify which parameters (such as lung function parameters) are associated with nocturnal hypercapnia or hypoxemia and/or poor sleep quality

Conditions

Interventions

DEVICE

SENTEC device

Nocturnal recording SAO2 and PtcCO2 and wrist movements by means of actigraphy

Sponsors & Collaborators

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Brigitte Fauroux, MD · Assistance Publique - Hôpitaux de Paris

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Primary Completion
2009-06-30
Completion
2009-06-30

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT00804661 on ClinicalTrials.gov