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To study the effect of Priyangwadi ointment with compare to Silver colloid ointment for the treatment of post operative Incision & drainage wound.

“RANDOMISED CONTROLLED CLINICAL TRIAL TO COMPARE THE EFFICACY OF EXTERNAL USE OF PRIYANGWADI OINTMENT WITH SILVER COLLOID OINTMENT IN THE MANAGEMENT OF VIDRADHI BHEDAN PASHCHAT VRAN"

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059793
Enrollment
38
Registered
2023-11-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: L029- Cutaneous abscess, furuncle and carbuncle, unspecified

Interventions

None listed

Sponsors

Tilak Ayurved Mahavidyalaya Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Post operated incised & drained wound of maximum size 1cm to 6cm & depth 6cm

Exclusion criteria

Exclusion criteria: Patient with tuberculosis, leprosy, HIV & HBsAg and metabolic disorders and infected wound.

Design outcomes

Primary

MeasureTime frame
Healthy healing wound with reducing the size of wound. With pain(shula), redness (Araktata), edges(vrana oshtha), granulation, tenderness (sparshasahatwa)Timepoint: Baseline 11th day

Secondary

MeasureTime frame
Healthy healing wound with reducing the size of wound. With pain(shula), redness (Araktata), edges(vrana oshtha), granulation, tenderness (sparshasahatwa)Timepoint: 2 to 3 weeks

Countries

India

Contacts

Public ContactDr Dhanraj Bhagwan Gaikwad

Tilak ayurved mahavidyalaya

Draj.gaikwad@gmail.com9422342048

Outcome results

None listed

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