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Antipyretic effect of paracetamol vs mefenamic acid in treatment of febrile children

Antipyretic effect of paracetamol vs mefenamic acid in treatment of febrile children- randomized control study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/12/016798
Enrollment
159
Registered
2018-12-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: R508- Other specified fever

Interventions

Intervention1: paracetamol: to assess time taken to decrease single episode of fever spike to normal range Intervention2: mefenamic acid and paracetamol: First group will receive paracetamol 15mg/kg/d

Sponsors

Dr Amruta Loya
Lead Sponsor
Dr Mohd Saeed Siddiqui
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Children between 6 months and 5years of age, of either sex and with a Axillary temperature of 38°C/100.4 F or above included in the study

Exclusion criteria

Exclusion criteria: If patient received any antipyretic drug in previous 6 hrs History of hypersensitivity to study medication patients receiving antibiotics Patients admitted in ICU Patients with active gastrointestinal bleeding Known coagulopathy Chronic renal, liver and cardiac failure Pt medicated with warfarin, heparin or any other anti hypertensives Any medication that could interfere with the study was not permitted during the study. Any clinical adverse event, serious illness or other medical condition in view of investigator/treating doctor, in which continued participation was not in the best interest of the subject Voluntary decision of legal guardian/patient to withdraw from the study Any patient who required the use of an unacceptable concomitant medication or intervention that interfered with the study If febrile seizure/convulsions occurred to the child during the study. If the patients temp does not drop to normal range , then patient will be excluded from the study If body temp increases above 104 degree farenheit or decreases below 96.5 degree farenheit.

Design outcomes

Primary

MeasureTime frame
To study the Antipyretic effect of Paracetamol and Mefenamic acid in treatment of febrile childrenTimepoint: 15mins

Secondary

MeasureTime frame
To assess the time taken to decrease the single episode of fever to normal range by Paracetamol[20mg/kg/dose] and Mefenamic acid.[6mg/kg/dose] To compare tolerability of Paracetamol and Mefenamic acid in children. To compare the effect of Paracetamol and Mefenamic acid in different intensities of fever. To know the duration of antipyretic effect of Paracetamol and Mefenamic acid. Timepoint: 15 mins

Countries

India

Contacts

Public ContactDr Amruta Loya

MGM Medical College and Hospital

drmdsaeed@gmail.com9890307150

Outcome results

None listed

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