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Effect of tepid sponging

Investigating the effect of tepid sponging along with acetaminophen versus acetaminophen alone for reducing body temperature in hospitalized febrile children, Sabzevar, Iran

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250605066077N1
Enrollment
326
Registered
2025-08-29
Start date
2025-07-23
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Children with fever. Fever, unspecified

Interventions

Intervention 1: Intervention group: Sterile gauze soaked in lukewarm tap water (temperature between 34-37°C) is placed on the forehead, chest, armpits, and thighs for 15 minutes. During this time, the

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Months to 11 Years

Inclusion criteria

Inclusion criteria: The child's age must be between one month and 11 years. The temperature in the larger armpit is equal to 37.8

Exclusion criteria

Exclusion criteria: Dehydration and lack of fluid therapy in the child Diagnosis of malignant hyperthermia, neurological disorders, and seizures in children Medical intervention that interferes with the study and occurs within three hours of acetaminophen administration (i.e., during the time when body wash is scheduled to be performed) Less than 4 hours until the next dose of fever reducer. Having a child vomit Seizures

Design outcomes

Primary

MeasureTime frame
Prescription acetaminophen dosage. Timepoint: At the moment of hospital admission at triage, at the moment of study entry by the researcher, and at 30, 60, and three hours after acetaminophen administration. Method of measurement: Dropper.

Secondary

MeasureTime frame
Body temperature. Timepoint: Both groups were recorded at the moment of arrival at the hospital at triage, at the moment of entry into the study by the researcher, and at 30, 60, and three hours after acetaminophen administration. Method of measurement: Celsius.;Length of hospitalization. Timepoint: Both groups were recorded at the moment of arrival at the hospital at triage, at the moment of entry into the study by the researcher, and at 30, 60, and three hours after acetaminophen administration. Method of measurement: By the hour.;Restlessness and crying. Timepoint: Both groups were recorded at the moment of arrival at the hospital at triage, at the moment of entry into the study by the researcher, and at 30, 60, and three hours after acetaminophen administration. Method of measurement: Using a questionnaire with options (none, low, severe).;Chills. Timepoint: Both groups were recorded at the moment of arrival at the hospital at triage, at the moment of entry into the study by the researcher, and at 30, 60, and three hours after acetaminophen administration. Method of measurement: Using a questionnaire with options (no, yes).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Sadr

Sabzevar University of Medical Sciences

msadr9561@gmail.com+98 51 4401 8301

Outcome results

None listed

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