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Management Of Navajwara or Acute fever with Jwarahara Mahakashaya Arka and Jwarahara Mahakashaya Ghan Vati

An Open Label Double Arm Randomized Comparative, Clinical, Study to Evaluate the Efficacy of Jwarhar Mahakashay Arka and Jwarhar Mahakashay Ghanvati in the Management of Navajwara with special reference to Acute Fever - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054987
Enrollment
64
Registered
2023-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: R509- Fever, unspecified

Interventions

None listed

Sponsors

Dean Faculty Of Ayurved Parul University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient of either gender suffering from fever of age 18 to 60 years. 2.Acute onset fever of 1 to 3 days. 3.Temp. between 98.9â??- 100.9â?? 4.Patient suffering from the symptoms 1. Swed avarodh(Suppression of perspiration), 2. Santap(Raised body tempture), 3. Sarvang Vedana(Bodyache) 5.Fever of acute onset without any complications i.e. shock, convulsions, 6.Patients who agree to participate and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Chronic fever associated with immuno compresive disorder like H.I.V, T.B. 2.Pregnant women and lactating women . 3.If body temperature exceeds beyond 101â??. 4.Any febrile condition of patients requiring an immediate intervention depending on history and general condition at the point of examination as Found by the investigator will be excluded from Study.

Design outcomes

Primary

MeasureTime frame
Effects on Navajvara on the basis of scale of Agnimandya, Angamarda, Swedavarodh,Pindikodwestan ,Shirashool. Timepoint: Assessment of baseline (temperature) 8 hours, 16 hours, 24 hours. Total study time 7 days & follow up 3 days

Secondary

MeasureTime frame
Effects on Navajvara on the basis of of Temperature (axillary body temperature in °F) CBC CRP ESR Urine Routine/Micro Timepoint: Assessment of baseline (temperature) 8 hours, 16 hours,24 hours. Total study 7 days follow up 3 days

Countries

India

Contacts

Public ContactDr Vishal Sheth

Parul Institute of Ayurved

dr.manurajgopal@gmail.com9481328930

Outcome results

None listed

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