Acute Effect of Sildenafil on Exercise Tolerance and Functional Capacity in COPD, IPF and Post Pneumonectomy Patients

Sponsor
Rabin Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT01382368
Collaborator
(none)
60
1
1
24
2.5

Study Details

Study Description

Brief Summary

  • Pulmonary diseases are increasingly important causes of morbidity and mortality in the modern world.

  • Sildenafil, an orally administered a phosphodiesterase type 5 (PDE-5) inhibitor, targets the nitric oxide (NO) pathway. The drug was first approved for the treatment of Pulmonary Arterial Hypertension (PAH) in 2005.

  • The aim of the suggested study is to examine the acute effect of oral intake of sildenafil on exercise tolerance and functional capacity in Chronic Obstructive Pulmonary Disease (COPD), Idiopathic pulmonary fibrosis (IPF) and post Pneumonectomy patients.

  • The investigators hypothesize that oral ingestion of sildenafil prior the exercise may enhance exercise tolerance and improve function in COPD, IPF and post Pneumonectomy patients.

  • Patients and Methods:

Sixty chronic lung disease patients males and females (aged 30 to 90 years) 20 COPD (GOLD III-IV) [9, 39] , 20 IPF and 20 post Pneumonectomy patients will be recruit to this study.

  • All subjects will carried out two maximal cardiopulmonary exercise tests (CPET) on bicycle ergometer in different days; 60 min after intake of placebo and 60 min after intake of 100 mg sildenafil (Pfizer, Sandwich, UK), in random order.

  • In first meeting prior exercise test at rest standard pulmonary function test, diffusion of CO, TLC and RV will be measured. In addition, Doppler Echocardiography and blood samples for NT-proBNP will be taken prior and post each CPET.

  • After 15-20 minute of passive recovery post exercise test all patients will perform 3 short functional tests including 6 minute walk test to assess functional capacity.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Acute Effect of Sildenafil on Exercise Tolerance and Functional Capacity in COPD, IPF and Post Pneumonectomy Patients
Study Start Date :
Sep 1, 2011
Anticipated Primary Completion Date :
Nov 1, 2012
Anticipated Study Completion Date :
Sep 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sildenafil

Drug: Sildenafil
Acute single dose of 100 mg of sildenafil. Oral intake in tablet form.

Outcome Measures

Primary Outcome Measures

  1. VO2 Peak [2-30 days between exercise tests]

  2. 6 min walk test [2-30 days between exercise tests]

    Distance walked in 6 min test

  3. Functional Tests [2-30 days between exercise tests]

    30 seconds chair stand test- number of repetitions in 30 sec 8-ft-up-and -go (agility and coordination)- number of sec that takes to complete the task.

Secondary Outcome Measures

  1. Pulmonary Arterial Pressure [2-30 days between exercise tests]

  2. NT-pro-BNP [2-30 days between exercise tests]

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients with severe COPD GOLD stage III- IV, FEV1 30-50% or less of predicted values, greater shortness of breath, reduced exercise capacity, repeated excretions and\ or with chronic respiratory failure [9, 39].

  2. IPF patients diagnosed essentially according to the American Thoracic and European Respiratory Societies (ATS-ERS) by clinical diagnostic criteria of: (a) High-resolution computed tomography (HRCT) demonstrating a pattern of "confident" or "possible" IPF (b) Abnormal pulmonary physiology with evidence of restriction and/or impaired gas exchange (can exist during exercise alone) (c) Exclusion of other known causes of interstitial lung disease (e.g.: connective tissue disease, environmental exposure,etc.)[31].

  3. Patients post Pneumonectomy more than 6 month from the amputation surgery for any diagnosis (Cancer, Trauma, and Infection- Bronchiectasis).

Exclusion Criteria:
  1. Patients with known sensitivity or contraindications to phosphodiesterase 5 (PDE-5) inhibitor therapies will be excluding from the study.

  2. Thromboembolic disease will be excluded by pulmonary CT-angiography or perfusion scan.

  3. Patients with a history of left-sided heart failure will be excluded.

  4. Patients will also exclude if they are on regular treatment with nitrates or PDE-5 inhibitors (Sildenafil, Tadalafil, Vardenafil).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Pulmonary Institute, Rabin Medical Center, Beilinson Hospital Petach Tikva Israel 49100

Sponsors and Collaborators

  • Rabin Medical Center

Investigators

  • Principal Investigator: Mordechai R Kramer, M.D, Rabin Medical Center, Belinson Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mordechai Kremer, Prof. Mordechai R. Kramer, Head of Pulmonary Institute, Rabin Medical Center
ClinicalTrials.gov Identifier:
NCT01382368
Other Study ID Numbers:
  • RMCBH116278 CTIL
First Posted:
Jun 27, 2011
Last Update Posted:
Nov 15, 2012
Last Verified:
Nov 1, 2012
Keywords provided by Mordechai Kremer, Prof. Mordechai R. Kramer, Head of Pulmonary Institute, Rabin Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 15, 2012