Trials / Completed
CompletedNCT00831376
Trough Bronchoprotection Conferred by Levosalbutamol and Racemic Salbutamol
A Proof of Concept Study to Evaluate the Trough Bronchoprotection Conferred by Chronic Dosing With Levosalbutamol and Racemic Salbutamol in Persistent Asthmatics
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- University of Dundee · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to compare the relative bronchoprotection (at trough) conferred by 2-week chronic dosing with levosalbutamol and racemic salbutamol in mild to moderate asthmatics. Patients will be preselected into two groups on the basis of their beta-2 adrenoreceptor polymorphisms. The investigators will evaluate if this has a differential effect on the bronchoprotection conferred by both formulations of salbutamol, as evidenced by a rebound in airway hyper-responsiveness, in order to determine whether any effect can be explained by the S enantiomer in the racemic formulation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | levosalbutamol | Patients will be asked to take two puffs four times a day for 2 weeks |
| DRUG | racemic salbutamol | Patients will be asked to take two puffs four times a day for 2 weeks |
| DRUG | placebo | Patients will be asked to take two puffs four times a day for 2 weeks |
Timeline
- Start date
- 2009-01-01
- Primary completion
- 2012-04-01
- Completion
- 2012-04-01
- First posted
- 2009-01-28
- Last updated
- 2019-04-12
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT00831376. Inclusion in this directory is not an endorsement.