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A Clinical Study To Evaluate The Effect Of Madhuyukta Sura Dressing In Clean Wound

Randomised Open Controlled Clinical Trial To Evaluate Efficacy Of Madhuyukta Sura In The Management Of Shuddha Vrana - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112739
Enrollment
55
Registered
2026-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: T758- Other specified effects of external causes

Interventions

None listed

Sponsors

Dr Praaad Balasaheb Laware
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Individual aged between 18 to 55 years irrespective of gender, socioeconomic status, religion,cast 2 Patients presenting with clean wound with wound size less than 5 5 1 cm in length breadth and height 3 NijVrana in Shuddha avastha 4 Dushta Vrana in Shuddha avastha

Exclusion criteria

Exclusion criteria: 1 Individual suffering from complex or chronic wound conditions 2 Known case of Uncontrolled diabetes mellitus 3 Known case of patients who are HIV Hbsag HCV positive 4 Patients presenting with following wound types Compound fracture with wound Ischemic ulcer Neurogenic ulcer Immunocompromised patients Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To study the Efficacy of madhuyukta sura in management of shuddhavranaTimepoint: 15 Days

Secondary

MeasureTime frame
To Evaluate The effect of Madhuyukta Sura and Povidone Iodine Dressing along with management of Shuddha Vrana within 15 days of treatmentTimepoint: To Evaluate The effect of Madhuyukta Sura and Povidone Iodine Dressing along with management of Shuddha Vrana within 15 days of treatment

Countries

India

Contacts

Public ContactPrasad Balasaheb Laware

Yashwant Ayurvedic College Post Graduate Training and Research Centre Kodoli

drsrinivast@gmail.com9359867241

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026