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Clinical Trials/NCT01869387
NCT01869387
Unknown
N/A

Improvement of Respiratory Muscle Function With Noninvasive Ventilation in Exacerbated COPD Patients Presenting Hypercapnic Respiratory Failure Without Acidosis

Parc de Salut Mar1 site in 1 country46 target enrollmentJune 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Sponsor
Parc de Salut Mar
Enrollment
46
Locations
1
Primary Endpoint
Respiratory muscle function.
Last Updated
12 years ago

Overview

Brief Summary

There is evidence that noninvasive mechanical ventilation (NIV) is effective in the treatment of severe exacerbations of COPD presenting respiratory acidosis.

The aim of the study is to evaluate the benefit of adding NIV to conventional treatment in patients with COPD exacerbation and hypercapnic respiratory failure without acidosis requiring hospital admission. It is known that NIV improves respiratory mechanics, so the primary outcome will be respiratory muscle function.

All patients admitted to the hospital for COPD exacerbation and hypercapnic respiratory failure without acidosis will be included for a period of 12 months. The patients will be randomized into two groups (conventional treatment or conventional treatment plus NIV). Clinical data, blood gases, muscle strength parameters will be collected at the inclusion time and 24h after starting NIV. Quality of life and hospital stay will be measured at discharge. All patients will be followed for a year.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
December 2015
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Parc de Salut Mar
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of COPD according to international guidelines ( GOLD)
  • COPD exacerbation requiring hospitalization
  • Initial blood gases: PaCO2\> 50 mm Hg and pH\> 7.
  • If the patient does not have COPD diagnosis at the time of inclusion, it could be included if the diagnosis is confirmed within three months after the exacerbation.

Exclusion Criteria

  • Patients with a pH below 7.35
  • Patients with intubation criteria
  • Other chronic respiratory diseases (fibrothorax, cystic fibrosis, significant ribcage alterations)
  • Neuromuscular Diseases
  • Significant associated chronic systemic diseases (severe liver disease, chronic renal failure requiring dialysis, severe heart disease and active neoplasia)
  • COPD exacerbation secondary to pulmonary embolism, pneumonia or pneumothorax
  • Patients in active treatment with CPAP or home ventilation

Outcomes

Primary Outcomes

Respiratory muscle function.

Time Frame: At baseline, at discharge (average of 8 days), 6 months and one year later.

Measurement of maximal inspiratory pressure and sniff nasal inspiratory pressure using a portable respiratory pressure meter.

Secondary Outcomes

  • Days of hospitalization.(At discharge (average of 8 days).)
  • Dyspnea scale questionnaire(At baseline, at discharge, 6 months and one year later.)
  • Quality of life(At baseline, 6 months and one year later.)
  • Blood gases(At baseline and at discharge (average of 8 days).)
  • Number of hospital readmissions in the next year(At one year after discharge (average of 8 days).)

Study Sites (1)

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