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To test if Paranthyadi Taila helps reduce pain and wound size in patients with infected wounds within 21 days.

An Exploratory Clinical Trial to study the efficacy of ParanthyadiTaila in the management of dushtavrana - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086682
Enrollment
63
Registered
2025-05-09
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: L089- Local infection of the skin and subcutaneous tissue, unspecified

Interventions

None listed

Sponsors

PDEAs College of Ayurved and Research Centre Nigi Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with symptom of Shula, Puyadi Strava. Age group between 18-60 yr K/C/O Bed sores Post operative infected wound / Infected traumatic wound Wound size Up to 9x9 cm

Exclusion criteria

Exclusion criteria: Non specific Non healing ulcers Gangrenous wounds K/C/O HIV,HbsAg,tuberculous positive,leprosy All Medico legal cases will be excluded

Design outcomes

Primary

MeasureTime frame
The effect of ParanthyadiTaila will be accessed for local application in dushtavrana assessment will be done by criteria like Vranatala (floor), Smell (gandha), discharge (strava), vrana kathinya, sthanik aushnya, pain, vrana pariman.Timepoint: Follow up with assessment of patient on 7th,14th,22nd day—

Secondary

MeasureTime frame
NATimepoint: NA—

Countries

India

Contacts

Public ContactDr Bharat K Oza

PDEAs College of Ayurved and Research Centre,Nigdi,Pune

drbharat_oza@yahoo.co.in9970254593

Outcome results

None listed

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