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Do phosphodiesterase-5 inhibitors improve exercise capacity in COPD patients with pulmonary hypertension?

Phase 2
Completed
Conditions
COPD with pulmonary hypertension
Signs and Symptoms
Other chronic obstructive pulmonary disease
Registration Number
ISRCTN10877141
Lead Sponsor
niversity of Dundee (UK)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
120
Inclusion Criteria

Current inclusion criteria as of 08/10/2012:
1. Male or female participants, aged between 35 to 85 inclusive
2. COPD
3. Forced Expiratory Volume in one second (FEV1) <80% predicted (protocol change approved 18/02/2011)
4. Right Ventricular Systolic Pressure (RVSP) >30mmHg and/or pulmonary acceleration time <120 ms

Previous inclusion criteria until 08/10/2012:
1. Male or female participants, aged between 35 to 85 inclusive
2. Diagnosis of COPD or Emphysema (diagnosis of emphysema removed due to an error in the original application)
3. Forced Expiratory Volume in one second (FEV1) <50% predicted
4. Smoker or ex-smoker with a history = 20 pack years (removed due to protocol change approved 23/01/2012)
5. Right Ventricular Systolic Pressure (RVSP) >30mmHg and/or pulmonary acceleration time <120 ms
6. Plasma Brain Natriuretic Peptide (BNP) level >25 pg/ml (removed due to protocol change approved 18/02/2011)

Exclusion Criteria

1. Pulmonary stenosis
2. Echo Left Ventricular (LV) outflow obstruction
3. LV systolic dysfunction (LVEF <45%)
4. Patients taking nitrates, nicorandil or doxazosin
5. Systolic blood pressure (BP) <90 mmHg, recent stroke, unstable angina, past history of non arteritic anterior ischaemic optic neuropathy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Six-minute walk distance test (6WMD) performed at baseline, 2 and 3 months
Secondary Outcome Measures
NameTimeMethod
Current secondary outcome measures as of 08/10/2012:<br>1. Quality of Life<br>1.1. St George's Respiratory Questionnaire (SGRQ)<br>1.2. SF-36<br>1.3. Minnesota Living with Heart Failure® questionnaire (MLHFQ) <br>2. Diffusing Capacity of the Lung for Carbon Monoxide (DLCO)<br>3. B-type Natriuretic Peptide<br>4. Echocardiogram Measurements<br>Outcomes assessed at baseline, 2 and 3 months with the exception of DLCO and echo which are performed at beginning and end only (protocol change approved 18/02/2011). <br><br>Previous secondary outcome measures until 08/10/2012:<br>Outcomes assessed at baseline, 2 and 3 months.
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