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investigation the effective of oral amoxicillin with half the therapeutic dose in reducing the hospitalization rate of patients with neuromuscular disease and cerebral palsy due to aspiration pneumonia during the years 1401-1402

Not Applicable
Recruiting
Conditions
Condition 1: Aspiration Pneumonia. Condition 2: Cerebral Palsy.
Pneumonitis due to solids and liquids
Cerebral palsy
Registration Number
IRCT20221126056619N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients aged between 6 months to 15 years suffering from severe neurological diseases and cerebral palsy undergoing related neurological treatments.
Patients who have presented with recurrent respiratory infections and have a previous history of at least one hospitalization due to aspiration pneumonia.
Patients who have been evaluated for demographic conditions, socioeconomic level, oral and dental nutrition status, care hygiene, cognitive status, movement and musculoskeletal conditions, and respiratory conditions, including dependence on respiratory devices.

Exclusion Criteria

Patients who do not tolerate the oral antibiotic (Amoxicillin) treatment or show gastrointestinal symptoms will be excluded from the study.
Any severe illness or medical condition that, in the opinion of the investigator, might interfere with the patient's participation in the study.

Study & Design

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