Skip to content

A Clinical study to evaluate the efficacy of Ingudi taila over Jatyadi taila in management of Dushta vrana (Chronic wound)

A controlled clinical study to evaluate the efficiency of Ingudi taila over Jatyadi taila in management of Dushta vrana (Chronic wound) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074694
Enrollment
40
Registered
2024-10-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: L979- Non-pressure chronic ulcer of unspecified part of lower leg

Interventions

None listed

Sponsors

Dr Anusha K
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient of age Group between 18-60 years, either of gender and having clinical features of Dushta vrana like Vedanayukta [Pain], Deergakalanubandi [chronic], Sravayukta [discharge] and dushta vrana having size less than 6x6cm [l x b] and 2cm depth.

Exclusion criteria

Exclusion criteria: Patients with HIV Positive, HBsAg Positive, known case of Tuberculosis, Uncontrolled Diabetes Mellitus, Malignant ulcers and Burns.

Design outcomes

Primary

MeasureTime frame
Assessment of Objective parameter- Pain, DischargeTimepoint: 3 weeks

Secondary

MeasureTime frame
Assessment of- Size, Depth of the cavity, Granulation tissueTimepoint: TOTAL STUDY DURATION PER PATIENT- 21 Days. TREATMENT DURATION- 15 Days. FOLLOW UP PERIOD- on 21st day. ASSESSMENT DONE ON- 1st day (Before treatment), 3rd day [During treatment], 7th day [During treatment], 15th day [After treatment] and 21st day [During follow up].

Countries

India

Contacts

Public ContactDr Geetanjali Hiremath

Shree Jagadguru Gavisiddeshwara Ayurvedic Medical College and Hospital, Koppal

sanjalihiremath@gmail.com7760346752

Outcome results

None listed

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