Respiratory Muscle Function in COPD Exacerbations

Sponsor
Parc de Salut Mar (Other)
Overall Status
Unknown status
CT.gov ID
NCT01869387
Collaborator
(none)
46
1
2
30
1.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Non-invasive ventilation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
46 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Improvement of Respiratory Muscle Function With Noninvasive Ventilation in Exacerbated COPD Patients Presenting Hypercapnic Respiratory Failure Without Acidosis
Study Start Date :
Jun 1, 2013
Anticipated Primary Completion Date :
Jun 1, 2015
Anticipated Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Standard treatment

Standard treatment consists in bronchodilator and parenteral corticosteroids and oxygen therapy.

Experimental: Standard treatment plus non-invasive ventilation

This arm consists in bronchodilator and parenteral corticosteroids and oxygen therapy plus non-invasive ventilation.

Device: Non-invasive ventilation

Outcome Measures

Primary Outcome Measures

  1. Respiratory muscle function. [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 Outcome Measures

  1. Days of hospitalization. [At discharge (average of 8 days).]

  2. Dyspnea scale questionnaire [At baseline, at discharge, 6 months and one year later.]

  3. Quality of life [At baseline, 6 months and one year later.]

  4. Blood gases [At baseline and at discharge (average of 8 days).]

  5. Number of hospital readmissions in the next year [At one year after discharge (average of 8 days).]

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of COPD according to international guidelines ( GOLD)

  • COPD exacerbation requiring hospitalization

  • Initial blood gases: PaCO2> 50 mm Hg and pH> 7.35.

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital del Mar (Servei de Pneumología) Barcelona Spain 08003

Sponsors and Collaborators

  • Parc de Salut Mar

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Parc de Salut Mar
ClinicalTrials.gov Identifier:
NCT01869387
Other Study ID Numbers:
  • CRISOL-MARTINA-2013
First Posted:
Jun 5, 2013
Last Update Posted:
Jun 5, 2013
Last Verified:
May 1, 2013

Study Results

No Results Posted as of Jun 5, 2013