Skip to content

A study to evaluate two drugs, Panchatikta Ghrita and Nalpamaradi Taila in patients with Vicharchika(Eczema)

Clinical Evaluation of Panchatikta Ghrita and Nalpamaradi Taila in the Management of Vicharchika(Eczema)

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022236
Enrollment
120
Registered
2019-12-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: L309- Dermatitis, unspecified

Interventions

Intervention1: Panchatikta ghrita internally and Nalapamaradi taila externally: Panchatikta ghrita 6 g twice daily internally(orally) with luke warm water for 12 weeks Nalapamaradi taila 20ml (approxi

Sponsors

Central Council for Research in Ayurvedic Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex with age between 18 and 60 years 2. Known cases of eczema (based on Hanifin and Rajka Criteria for Atopic Dermatitis/ Atopic Eczema). 3. Patients willing and able to participate in the study

Exclusion criteria

Exclusion criteria: 1. Patient with Status Eczematous condition. 2. Patient with poorly controlled Hypertension ( >160/100 mmHg) 3. Patient with uncontrolled Diabetes Mellitus having HbA1C > 8% 4. Patient on medication with corticosteroids, phototherapy, biologics, antidepressants and any other drugs that may have an influence on the outcome of the study. 5. Alcoholic and/or drug abuser 6. Symptomatic patients with clinical evidence of heart failure. 7. Known case of HIV and AIDS. 8. Known case of Malignacy. 9. Patienttaking participation in any other clinical trial. 10. Woman who are planning for conception/pregnant or lactating. 11. Patientwith concurrent serious hepatic disorders (defined as aspartate amino (AST) and/ or Alanine AminoTransferase(ALT) >2times upper normal limit or Renal Disorders (defined as S. Creatinine >1.2mg/dl), Severe pulmonary Dysfunction (uncontrolled Bronchial Asthma and /or Chronic obstructive Pulmonary Disease (COPD). 12. H/o hypersensitivity to any of the trial drugs or their ingredients. 13. Patient who have completed participation in any other clinical trial during the past three months. 14. Any other condition which the Investigator thinks may jeopardize the study.

Design outcomes

Primary

MeasureTime frame
Change in Eczema Area Severity Index score (EASI) Change in Patient Oriented Eczema measure (POEM) Change in Dermatology life Quality Index (DLQI ) Questionnaire score Timepoint: At Baseline, 14th day, 28th day, 42th day, 56th day, 70th day, 84th day and 112th day

Secondary

MeasureTime frame
Change in Signs & Symptoms.Timepoint: At Baseline, 14th day, 28th day, 42th day, 56th day, 70th day, 84th day and 112th day

Countries

India

Contacts

Public ContactMidhuna Mohan K

Regional Ayurveda Research Institute for Skin Disorders, Vijayawada under CCRAS

midhunamohan@gmail.com9447894680

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 22, 2026