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Completed

NCT Number: NCT00405665

The Short Term Safety and Efficacy of Inhaled L-arginine in Patients With Cystic Fibrosis

The objective of this trial is to determine the safety and effect on pulmonary function of 14 days of inhaled L-arginine versus placebo administered over a period of 14 days in a cohort of CF patients.

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Key information

Age range

14 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

St. Michael's Hospital, Toronto, Ontario, Canada

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About this study

Despite the inflammatory nature of lung disease in CF, nitric oxide (NO) formation as well as the expression of NOS2 has been found to be decreased in CF airways. While the reasons for impaired airway NO formation remain incompletely understood, there is evidence that low NO formation contributes to lung pathophysiology in CF. Constitutive endogenous formation of Nitric oxide (NO) in airways is thought to play a role in neurotransmission, smooth muscle relaxation and bronchodilation. Previous animal experiments have shown that the addition of L-arginine, the precursor of enzymatic NO formation, resulted in a significantly greater relaxation of tracheas. There is also evidence that a single dose of inhaled L-arginine improves pulmonary function in CF. In this study we will assess the effect of L-arginine inhalation on lung function, nitric oxide formation, airway inflammation and bacterial infection in CF patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of CF as defined by two or more clinical features of CF and a documented sweat chloride concentration > 60 mEq/L and/or two well characterized disease causing CFTR gene mutations
  • 14 years of age and older at enrollment
  • Clinically stable at enrollment
  • Ability to comply with medication use, study visits and study procedures
  • FEV1 % predicted > 40% < 80 % as calculated by reference equations

Exclusion criteria

  • Respiratory culture positive for: B. cepacia complex within past year or at screening
  • Use of systemic corticosteroids within 30 days of screening
  • Use of intravenous antibiotics or oral quinolones within 14 days of screening
  • History of biliary cirrhosis, portal hypertension, or splenomegaly
  • Other major organ dysfunction
  • History of lung transplantation or currently on lung transplant list
  • Supplemental oxygen therapy
  • Oxygen saturation < 95 % on room air
  • Positive pregnancy test at screening
  • Investigational drug use within 30 days of screening
  • History of alcohol, illicit drug or medication abuse within 1 year of screening
  • Acute respiratory symptoms
  • Inability to take any form of bronchodilator
  • Wheezing at the time of study

Treatment and study plan

L-arginine

Drug

Group 1 will receive the active treatment followed by the inactive treatment. The active treatment phase will consist of L-arginine 250 mg/ml dispensed in 2.2 ml vials, from which the patient will take 2ml (500mg) and dilute with 3ml of sterile water to give 5ml of a 100mg/ml solution. Dosing in the inactive treatment phase will consist of a placebo of similar osmolarity and appearance will be formulated and dosed in a similar fashion. It will consist of 2.2ml vials of 1110mmol/L hypertonic saline. Again, the patient will take 2ml and dilute with 3ml of sterile water to give a 445mmol/L solution which has similar tonicity (10%) to the L-arginine. Both treatment phases will be administered by inhalation with a PARI eFLOW device.

Primary outcomes

  1. Change in FEV1 (in liters) from baseline

    Time frame: At the end of the 14 day treatment period

  2. Adverse events such as gastrointestinal complaints, wheezing, hepatitis or shortness of breath

    Time frame: 70 weeks

Secondary outcomes

  1. Change in FVC and change in FEV25-75 from baseline to completion of the 2 week treatment period.

    Time frame: Will be measured at the end of the 14 day treatment period

  2. Change in exhaled nitric oxide (FeNO)

    Time frame: 70 days

  3. Changes in inflammatory markers in sputum from baseline including neutrophils (sputum), neutrophil elastase (sputum) and interleukin (IL)-8 concentrations (sputum).

    Time frame: Will me measured at the end of the 14 day treatment period

  4. Changes in sputum concentrations of L-arginine metabolites

    Time frame: 70 days

Sponsors and collaborators

Lead sponsor

The Hospital for Sick Children

Other

Registry information

Official study title

Pilot Study of the Short Term Safety and Efficacy of Inhaled L-arginine in Patients With Cystic Fibrosis

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Nov 30, 2006
Registry last updated
Sep 2, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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