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ACE inhibitors to augment the effects of pulmonary rehabilitation in COPD

ACE inhibitors to augment the effects of pulmonary rehabilitation in COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN79038750
Enrollment
80
Registered
2012-11-29
Start date
2012-12-01
Completion date
Unknown
Last updated
2016-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD Respiratory Chronic obstructive pulmonary disease, unspecified

Interventions

Treatment will with 10mg enalapril or matched placebo once daily. Drug and placebo will be encapsulated by Royal Free Pharmacy. Drug will be dispensed from the pharmacy at Royal Brompton and Harefield

Sponsors

Imperial College London (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults with GOLD stage II-IV COPD and a clinical indication for pulmonary rehabilitation (MRC score of 3 or more or functionally limited)

Exclusion criteria

Exclusion criteria: 1. Clinically unstable patients (within one month of exacerbation) 2. Those with a permanent pacemaker (which is a contraindication to magnetic stimulation), or significant co-morbidity 3. Patients with an accepted indication for ACE inhibition (left ventricular dysfunction, diabetes) or a contraindication such as renovascular disease 4. Creatinine clearance (estimated) <50) 5. Hypotension 6. Use of anticoagulants (contra-indication to biopsy) or ACE-I or ATII receptor antagonists 7. Allergy to ACE-inhibitors 8. Pregnancy

Design outcomes

Primary

MeasureTime frame
Increase in peak workload achieved on a cycle ergometer following a rehabilitation program compared between enalapril and placebo treated patients.

Secondary

MeasureTime frame
1. Quadriceps strength 2. Six minute walk distance 3. HRQOL (CAT score) 4. Physical activity level (SenseWear armband)

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026