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Effect of Two Ayurvedic Applications on scorpoin Bite:A Comparative Study

A Comparative Clinical Trial To Evaluate The Effect Of Paravathasakruthadi Lepa Against Sigrupunarnavadi Lepa In Vrishika Damsa. - NILL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/092049
Enrollment
40
Registered
2025-07-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: T632- Toxic effect of venom of scorpion

Interventions

None listed

Sponsors

SELF
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 History of Vrischika damsa within 48 hours 2Participants of age group 18-60 years, irrespective of gender, caste, religion, or economic status 3 Participants with any one or more of following symptoms pain, burning sensation, erythema, swelling

Exclusion criteria

Exclusion criteria: Participants who have already undergone treatments for this condition. 1 Participants presenting complication like cardiac arrythmia, shock, 2 pregnant women and lactating mother. 3 Participants with chronic kidney disease. Participants aged below 18 years.

Design outcomes

Primary

MeasureTime frame
To analyze the effect of Paravathasakruthadi lepa on the management of vrischika damsa along with the internal administration of Dasanga agada. To compare the effects of Paravathasakruthadi lepa against Sigrupunarnavadi lepa along with Dasanga agada in the management of vrischika damsa. Timepoint: out come will be assessed at baseline day 3rd day 5th day .Final outcome measured at 18 months.

Secondary

MeasureTime frame
To compare the effect of Paravathasakruthadi lepa against Sigrupunarnavadi lepa along with Dasanga agada internally in the vrischika damsaTimepoint: 18 MONTHS

Countries

India

Contacts

Public ContactVidya K M

MVR AYURVEDA MEDICAL COLLEGE

dr.jayasmitha@gmail.com8714498512

Outcome results

None listed

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