Last updated: 11/07/2018 13:26:30

A Randomised, Double-Blind, Double-Dummy, Multicentre, Parallel Group Study to Assess the Efficacy and Safety of Oral Augmentin SR, Two Tablets Equal to 2000/125mg, Twice Daily for 10 Days Versus Levofloxacin (Levaquin) 500mg Once Daily for 10 Days in the Treatment of Adults with Acute Bacterial ...

GSK study ID
25000/550
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: A Randomised, Double-Blind, Double-Dummy, Multicentre, Parallel Group Study to Assess the Efficacy and Safety of Oral Augmentin SR, Two Tablets Equal to 2000/125mg, Twice Daily for 10 Days Versus Levofloxacin (Levaquin) 500mg Once Daily for 10 Days in the Treatment of Adults with Acute Bacterial ...
Trial description: A Randomised, Double-Blind, Double-Dummy, Multicentre, Parallel Group Study to Assess the Efficacy and Safety of Oral Augmentin SR, Two Tablets Equal to 2000/125mg, Twice Daily for 10 Days Versus Levofloxacin (Levaquin) 500mg Once Daily for 10 Days in the Treatment of Adults with Acute Bacterial ...
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:
File T, Jacobs MR, Poole MD, Wynne B. Outcome of treatment of respiratory tract infections due to Streptococcus pneumoniae, including drug-resistant strains, with pharmacokinetically enhanced amoxycillin/clavulanate. Int J Antimicrob Agents 2002; 20(4): 235–47.
File T, Jacobs MR, Poole MD, Wynne B. Clinical efficacy of pharmacokinetically enhanced amoxicillin/clavulanate (AMX/CA) vs comparators against Streptococcus pneumoniae (Sp) in respiratory tract infections (RTIs). Abstracts from the 2nd Forum on Respiratory Tract Infections, Monte Carlo, Monaco. February 2002, page 62, Abstract P4.
File T, Jacobs MR, Poole MD, Wynne B. Pharmacokinetically enhanced amoxicillin/clavulanate against Streptococcus pneumoniae (Sp) in respiratory tract infections (RTIs). Abstracts from the 42nd Interscience Conference on Antimicrobial Agents and Chemotherapy, San Diego, USA. September 2002, page 359, Abstract L-990.
Garau J, File T, Jacobs MR, Poole MD, Wynne B, The 546–551, 566, 557 and 592 Clinical Study Groups. Efficacy of amoxicillin/clavulanate (AMX/CA) 2000/125 mg b.i.d. against Streptococcus pneumoniae non-susceptible to AMX. Abstracts from the 4th International Meeting on the Therapy of Infections, Florence, Italy. October 2002, page 71, Abstract A5.
Medical condition
Sinusitis
Product
amoxicillin/clavulanic acid
Collaborators
Not applicable
Study date(s)
October 1999 to February 2000
Type
Not applicable
Phase
3

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

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
2000-17-02

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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A Randomised, Double-Blind, Double-Dummy, Multicentre, Parallel Group Study to Assess the Efficacy and Safety of Oral Augmentin SR, Two Tablets Equal to 2000/125mg, Twice Daily for 10 Days Versus Levofloxacin (Levaquin) 500mg Once Daily for 10 Days in the Treatment of Adults with Acute Bacterial ..., Trial ID 25000%2F550 | GSK