A study to compare the efficacy of sarivadi kashaya and parpatadi kashaya as gudavarti(suppository) in jwara santapa(pyrexia) in childre
Phase 3
- Conditions
- Health Condition 1: 3- Administration
- Registration Number
- CTRI/2024/07/070206
- Lead Sponsor
- Dr Parvathy B Geethakumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects with pyrexia with an axillary temperature ranging from 99.80°F to 103.0°F (low to moderate pyrexia). Subjects in whom parents are willing to sign the written consent form will be included.
Exclusion Criteria
Subjects who present with high-grade fever and subjects with a history of febrile seizures, epilepsy, or meningitis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Significant decrease in Jwara santapa (pyrexia) assessed based on GRASP fever chart.Timepoint: At 0-30 minutes,60 minutes,120minutes and 180 minutes after administration of gudavarti.
- Secondary Outcome Measures
Name Time Method Generation of in - depth analysed data on the different aspect of the disease- Jwara & generation of data on possible unexpected drug reactions which might occur during the study duration. <br/ ><br>Timepoint: 3 hours