PER-002-00
Completed
未知
Comparative study in pharyngitis and / or acute tonsillitis of Cephalexin (Keflex) versus Amoxicillin
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- ELI LILLY INTERAMERICA INC.,
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients from 2 years to 12 years of age.
- •Diagnosis of acute pharyngitis or acute tonsillitis (\<7 days duration)
- •Rapid Stret positive test before starting treatment.
- •The parent or legal representative must sign an informed consent document approved by a CE (Ethics Committee).
- •The investigator will try to select those patients with a history of complying with the instructions received.
Exclusion Criteria
- •Patients whose symptoms are due to evident viral infection of the upper respiratory tract.
- •Researchers and their immediate family members are not allowed to be subjects or patients in studies sponsored by Lilly. As an immediate family member, the researcher´s spouse, parents, children, grandparents or grandchildren are defined.
- •People who have previously completed this study or have withdrawn from it will not be eligible to participate in this study.
- •Reaction of severe hypersensitivity prior to cephalosporins or penicillin.
- •Administration of systemic antibiotics in the 7 days prior to randomization.
- •Inability to go to valuation consultation.
- •Concomitant use of probenecid or concomitant treatment with corticosteroids.
- •History of significant renal deterioration.
- •Any condition that, in the opinion of the investigator, could impede the evaluation of the response.
- •Patients who have received an agent in research (a drug that has not been approved for sale in the countries in which this study is conducted) as participants in a study, in the last 30 days.
Outcomes
Primary Outcomes
Not specified
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