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Nitric Oxide (NO) Donors and Inhibitors Study: Study to Evaluate L-Arginine and Aminoguanidine in Asthmatic Subjects

A Double Blind, Crossover Placebo-controlled Study to Evaluate the Effect of L-arginine and Aminoguanidine on Bronchial, Alveolar and Nasal NO and NO Metabolites

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00159380
Enrollment
16
Registered
2005-09-12
Start date
2003-09-30
Completion date
2005-03-31
Last updated
2019-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma

Brief summary

The primary aim of this study is to investigate the effects of oral and inhaled administration of L-arginine and of inhaled aminoguanidine on bronchial and alveolar exhaled NO and NO metabolites in exhaled breath condensate, saliva and nasal lavage fluid in normal and asthmatic subjects.

Detailed description

Nitric oxide (NO) is produced by a variety of cells within the respiratory tract, particularly airway epithelial cells, and its increased concentration in asthma is likely to derive from inducible NO synthase (iNOS) expressed in inflamed airways. To evaluate whether an increased bronchial flux of NO (ie, airway wall NO flux \[Jno\] in picoliters per second) produced in the large airways is due to an enzyme overexpression, we administered a relatively selective iNOS inhibitor, aminoguanidine, by nebulization in a double-blind, placebo-controlled manner in asthmatic and healthy subjects and also investigated whether the same concentration of inhibitor has any effect on NO produced in the peripheral lungs (ie, alveolar NO concentration \[Calv\] in parts per billion \[ppb\]) or on the diffusing capacity of NO (Dno) \[in picoliters per second-1 per ppb-1) in the airways. Aminoguanidine administration resulted in a significant reduction in Jno compared with administration of the saline solution control in eight healthy subjects and in eight patients with asthma but caused no significant changes in Calv or in Dno in either group.

Interventions

DRUGPlacebos

2ml

Sponsors

Imperial College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
21 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy non-smokers (n=10): * Nonatopic subjects (exhaled NO greater than or equal to 10 ppb; flow 50 ml/s) * Normal spirometry * Able to comprehend and grant a written informed consent Asthmatic subjects (n=15): * Forced expiratory volume in one second (FEV1) of no less than 70% of predicted (exhaled NO greater than or equal to 15 ppb; flow 50 ml/s) * Clinically stable (steroid-naïve or taking no \> 600 mcg/day of inhaled steroids) * Able to comprehend and grant a written informed consent

Exclusion criteria

* Currently smoking * Any lung disease other than asthma which may interfere with the study * Treatment within the last 4 weeks with oral steroids * Respiratory infection within 4 weeks prior to entry into the trial * Females who are pregnant or lactating * History of current or past drug or alcohol abuse

Design outcomes

Primary

MeasureTime frameDescription
Bronchial exhale nitric oxide6 hoursBronchial exhale nitric oxide (JNo) assessed by chemo luminescence
Peripheral exhaled nitric oxide6 hoursPeripheral exhaled nitric oxide(CALV) assessed by chemo luminescence

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026