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Comparison of the effectiveness of Manjishthasiddha Ghrita and Durvadya Taila for treatment of Vicharchika in children of age group 1-12 years.

A randomised comparative clinical study to evaluate the efficacy of external application of Manjishthasiddha Ghrita and Durvadya Taila in the management of Vicharchika in children of age group 1-12 years. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078528
Enrollment
60
Registered
2024-12-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: L00-L08- Infections of the skin and subcutaneous tissue

Interventions

None listed

Sponsors

PDEAs College of Ayurved and Research Centre, Nigdi, Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient having symptoms of Vicharchika mentioned in ayurvedioc text are- Raaji, Ruja, Kandu, Rukshata. Two or more of these symptoms should be present. 2. Children between the age group of 1 year to 12 years irrespective of sex

Exclusion criteria

Exclusion criteria: 1.Weeping eczemas, infected lesion will be excluded from the study. 2.Lichenified skin changes. 3.Children having acute febrile illness, acute respiratory infections or any disorders will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
To study the efficacy pf external application of Manjisthasiddha Ghrita and Durvadya Taila three times a day for 7 days in the treatment of Vicharchika in children of age group 1-12 years.Timepoint: 7 days treatment with follow up on 7th day with window period of +/- 3 days.

Secondary

MeasureTime frame
To observe adverse effects if anyTimepoint: 7 days treatment with follow up on 7th day

Countries

India

Contacts

Public ContactDr Prashant M Wankhede

PDEAs College of Ayurved and Research Centre

dr.prash30@gmail.com9970157701

Outcome results

None listed

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