Health Condition 1: J398- Other specified diseases of upperrespiratory tract
Conditions
Interventions
Intervention1: Co-Amoxyclav: Oral Co-Amoxyclav 625mg Three times a day for 7 days
Control Intervention1: Co-Amoxyclav: Co-Amoxyclav 625mg three times a day for 7 days
Control Intervention2: Cefpodoxim
Sponsors
Dr Nadeem Ahmed
Eligibility
Inclusion criteria
Inclusion criteria: A written consent for participation in the study. Patients suffering from acute uncomplicated bacterial tonsillitis.
Exclusion criteria
Exclusion criteria: Age below 18 years Viral Tonsillitis Tonsillitis with complications Tonsillitis with co existing lower respiratory tract infection Sinusitis Patients with renal and hepatic dysfunction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparative efficacy and safety of co-amoxyclav, cefpodoxime proxetil, and levofloxacin in patient with acute uncomplicated bacterial tonsillitisTimepoint: 3 days, 5 days, 7 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparative efficacy and safety of co-amoxyclav, cefpodoxime proxetil, and levofloxacin in patient with acute uncomplicated bacterial tonsillitisTimepoint: 3 days, 5 days, 7 days | — |
Countries
India
Contacts
Public ContactDr Nadeem Ahmed
Santosh Deemed to be University
Outcome results
None listed