Clinical Trials Directory

Trials / Completed

CompletedNCT00655928

Modulation of Lung Injury Complicating Lung Resection

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
52 (actual)
Sponsor
Imperial College London · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether N-acetylcysteine given intravenously 1 day pre-operatively is effective in preventing inflammation in the lungs, as measured by tests on blood, breath and lung specimens, in patients undergoing surgery to remove a portion of lung.

Detailed description

Acute lung injury occurs following lung resection in about 5% cases, and has a high mortality of around 50%. Management of these patients is largely supportive. Even in patients who do not develop clinical evidence of acute lung injury, markers of inflammation and oxidative stress are present in blood and exhaled breath condensate after lung resection. The purpose of this randomised double-blind placebo-controlled study is to determine whether lung injury can be prevented by pre-administration of N-acetylcysteine.

Conditions

Interventions

TypeNameDescription
DRUGN-acetylcysteineN-acetylcysteine 240mg/kg in 1 litre 0.9% saline intravenous over 12 hours pre-operatively
DRUG0.9% saline0.9% saline 1 litre intravenous over 12 hours pre-operatively

Timeline

Start date
2007-08-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2008-04-10
Last updated
2020-02-05
Results posted
2019-09-23

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00655928. Inclusion in this directory is not an endorsement.