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Clinical Trials/NCT00775710
NCT00775710
Completed
Phase 4

A Randomized Controlled Trial Comparing Two Protocols to Withdraw Non-invasive Ventilation (NIV) After an Episode of Hypercapnic Respiratory Failure

Hospital Clinic of Barcelona3 sites in 1 country128 target enrollmentMarch 2006
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ConditionsHypercapnic Respiratory Failure

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Hypercapnic Respiratory Failure
Sponsor
Hospital Clinic of Barcelona
Enrollment
128
Locations
3
Primary Endpoint
New episode of hypercapnic respiratory failure after discontinuation of non-invasive ventilation
Status
Completed
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of the study is to determine the optimal method to withdraw non-invasive ventilation after an episode of hypercapnic respiratory failure.

Registry
clinicaltrials.gov
Start Date
March 2006
End Date
August 2010
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Acute hypercapnic respiratory failure.
  • •Use of NIV to treat respiratory failure.
  • •Persistence of hypercapnia after discontinuation of NIV

Exclusion Criteria

  • •Facial or cranial trauma or surgery,
  • •Recent gastric or esophageal surgery,
  • •Active upper gastrointestinal bleeding,
  • •Excessive amount of respiratory secretions,
  • •Tracheostomy
  • •Lack of cooperation

Outcomes

Primary Outcomes

New episode of hypercapnic respiratory failure after discontinuation of non-invasive ventilation

Time Frame: At the end of enrollment time

Secondary Outcomes

  • Incidence of long term dependency on non-invasive ventilation(At the end of enrollment time)
  • Hospital and 6-month survival(At the end of enrollment time)

Study Sites (3)

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