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study to improve treatment outcomes of Brain Fever(acute encephalitis syndrome) in children

PENTOXIFYLLINE AS AN ADD ON THERAPY IN CHILDREN WITH ACUTE ENCEPHALITIS SYNDROME - AN OPEN LABEL RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044977
Enrollment
48
Registered
2022-08-26
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G02- Meningitis in other infectious andparasitic diseases classified elsewhere

Interventions

Intervention1: Drug Pentoxifylline: Tab Pentoxifylline at 20 mg/kg/day divided into 3 doses for 3 days (tablet to be crushed and mix with water and to be given through nasogastric tube). Control Inter

Sponsors

All India Institute of Medical Sciences Bhubaneswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children between 1 month and 14 years of age admitted to the IPD and PICU, dept. of paediatrics, All India institute of medical sciences, Bhubaneswar during the study period if they satisfy case definition of AES as per NVBDCP(national vector Borne disease control programme)guideline of India and have baseline GCS of � 12

Exclusion criteria

Exclusion criteria: 1. Duration of illness > 14 days at presentation 2. Known bleeding disorder 3. Vasculitis 4. Cerebral hemorrhage 5. Retinal Hemorrhage

Design outcomes

Primary

MeasureTime frame
Mean Time (hours) required to attain normal GCS or improvement by score of 3 as per pediatric GCS for � 2 years, and standard GCS for 2-14 years old child after initiation of treatment. Timepoint: every 6th hourly GCS will be assessed, starting from the time of 1st dose of intervention/ standard care till attainment of normal GCS or improvement of GCS by 3.

Secondary

MeasureTime frame
1. Adverse effects of Pentoxifylline. 2. Any change in the frequency of common Sequelae of AES (hearing problems, visual disturbance, and motor abnormality)Timepoint: At 1 month and 3 months of discharge

Countries

India

Contacts

Public ContactYATHEESH K S

All India Institute Of medical Sciences, Bhubaneswar

dr.dwibedi@gmail.com9438333001

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026