Although pulmonary hypertension (PH) is a quite frequent complication of advanced pulmonary diseases, and it is an independent prognostic factor, until now no evidence-based treatment approach exists for those patients. This study will address if the drug sildenafil can lower pulmonary vascular resistance in patients with significant pulmonary hypertension (high blood pressure in the lungs) associated to chronic obstructive pulmonary disease (COPD). It will see if this treatment can improve effort capacity, quality of life without causing a deterioration in pulmonary gas exchange (mainly arterial oxygenation). Patients 18 years of age and older with moderate COPD and pulmonary hypertension (mean pulmonary arterial pressure \>30 mmHg) may be eligible for this study. Participants are randomly assigned to receive sildenafil or placebo (pill with no drug) for 16 weeks. Before starting treatment (baseline), and a the end of the study, the patients have a comprehensive assessment including: * a chest x-ray and CT scan (only at baseline); * pulmonary function tests to measure how much air the patient can breathe in and out, and the capacity of diffusion of gases; * arterial blood gases analysis (for safety reason this examination is performed at baseline, before the randomization after one hour from the administration of a tablet (20 mg) of sildenafil, and every month) * an echocardiogram (heart ultrasound) (only at baseline); * a 6-minute walk test to measure exercise capacity; * a quality-of-life assessment (SF-36 questionnaire) * a right heart catheterization to evaluate the severity of hypertension At the end of the 16-week period, patients may opt to continue to receive sildenafil and monitoring in an open-label phase of the study for up to 1 year.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
32
sildenafil 20 mg t.i.d. compared to placebo 20 mg t.i.d - 16 weeks treatment
placebo t.i.d.
Pulmonary Unit - Azienda Ospedaliera Ospedale Niguarda Ca' Granda
Milan, Milano, Italy
ACTIVE_NOT_RECRUITINGPulmonary Diseases Clinic - Azienda Ospedaliera Universitaria - Policlinico di Modena
Modena, Modena, Italy
ACTIVE_NOT_RECRUITINGPulmonary Clinic - Federico II University - Azienda Ospedaliera V. Monaldi
Napoli, Napoli, Italy
RECRUITINGThoracic Surgery Clinic - Azienda Ospedaliera di Padova
Padua, Padova, Italy
ACTIVE_NOT_RECRUITINGDept. of Medicine - Pulmonary Medicine - IsMeTT
Palermo, Palermo, Italy
RECRUITINGPulmonary Diseases Clinic - Fondazione IRCCS Policlinico San Matteo
Pavia, Pavia, Italy
RECRUITINGPulmonary Hypertension Center - Policlinico Umberto I
Rome, Rome, Italy
RECRUITINGUniversity Pulmonary Unit - Azienda Ospedaliera Universitaria Senese
Siena, Siena, Italy
RECRUITINGPulmonary Unit - Azienda Ospedaliera Universitaria San Giovanni Battista
Torino, Torino, Italy
RECRUITINGPulmonary Unit - Azienda Ospedaliera Universitaria Ospedali Riuniti di Trieste
Trieste, Trieste, Italy
RECRUITINGPulmonary vascular resistance (PVR)
PVR are measured by right cath study as the following formula: PVR= (mean pulmonary arterial pressure-pulmonary arterial wedge pressure)/cardiac output
Time frame: 16 weeks
Arterial blood gas analysis
Time frame: 16 Weeks
Pulmonary function - Borg scale
The dyspnea is assessed by an analogic scale from 0 (no dyspnea) to 10 (very severe dyspnea)
Time frame: 16 Weeks
Pulmonary function - Bode Index
The BODE Index is a composite marker of disease taking into consideration the systemic nature of COPD: FEV1% pred = predicted amount as a percentage of the forced expiratory lung volume in one second; 6MWD = six minute walking distance; MMRC = modified medical research council dyspnea scale; BMI = body mass index.
Time frame: 16 Weeks
Functional capacity - Quality of Life
Quality of Life is assessed by a standardized questionnaire (SF-36 questionnaire) at baseline and the end of study
Time frame: 16 Weeks
Functional capacity testing - 6 Minutes walking test
The six-minute walk test is performed in a straight corridor (length 25-30 meters) in the same environmental conditions
Time frame: 16 Weeks
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