Last updated: 11/07/2018 19:18:30
A Comparison of Salmeterol Versus Theophylline Versus Salmeterol Plus Theophylline in COPD Patients
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A Comparison of Salmeterol Versus Theophylline Versus Salmeterol Plus Theophylline in COPD Patients
Trial description: A Comparison of Salmeterol Versus Theophylline Versus Salmeterol Plus Theophylline in COPD Patients
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Abstract: Giessel, G MD; ZuWallack, R MD; Cook, C MD; Anderson, W MD; Reilly, D MD; Emmett, A MD, and Rickard, K MD, 63336. A Comparison of Serevent and Theophylline on Pulmonary Function in COPD Patients [4/23/1999]. 4/28/1999: Giessel, G MD; ZuWallack, R MD; Cook, C MD; Anderson, W MD; Reilly, D MD; Emmett, A MD, and Rickard, K MD, 3/9/2003. American Lung Association/American Thoracic Society 1999 International Conference; San Diego, CA; USA. 1999 Apr 23; c1999.
Anderson W. Fling M Xue ZY, et al. Frequency and Function of Beta2 Adrenergic Receptor Polymorphisms in COPD, ATS, 1999 (Abstract/Poster)
Giessel G, ZuWallack R, Cook C, et al. A Comparison of Serevent and Theophylline on Pulmonary Function in COPD Patients, ATS, 1998 (Abstract/Poster)
Knobil K, Emmett A, Reilly D, et al. Combination Therapy with Salmeterol and Theophylline for COPD, ATS, 2000 (Abstract/Poster)
ZuWallack R, Mahler D, Reilly D, et al. Salmeterol Plus Theophylline Combination Therapy in the Treatment of COPD. Chest, Vol 119:1661-1670, June 2001
Medical condition
Asthma
Product
salmeterol
Collaborators
Not applicable
Study date(s)
May 1997 to June 1998
Type
Not applicable
Phase
4
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1998-23-06
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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