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A clinical trial to study efficacy of high dose of oral and parenteral Amoxycillin-Clavunate in severe pneumonia in chidren under five years of age.

Phase 4
Completed
Conditions
Health Condition 1: null- Children with severe pneumonia aged 2-59 months.
Registration Number
CTRI/2010/091/000341
Lead Sponsor
Dr Sadbhavna Pandit
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
165
Inclusion Criteria

Patients in age group 2-59 months with a diagnosis of Severe Pneumonia.

Severe pneumonia defined as Fever,Cough,Fast breathing (Respiratory rate more than 50 in age group 2-12 months and > 40 in 12-59 months) and Chest Indrawing.

Exclusion Criteria

Inability to take orally
Bronchial Asthma
Allergy to Penicillin
Very Severe Pneumonia
Grade3,4 PEM
Pleural Effusion
Congenital Heart Disease
Tuberculosis
Shock
Immunocompromised Patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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