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"Clinical trial of some Ayurvedic drugs and special diets in the management of Psoriasis"

â??Clinical evaluation of efficacy of the Panchtiktaguggulu Ghrita and Brihan marichadya Taila in the management of Psoriasis w. s. r. to Pathya - Apathyaâ?? - CEEPBMP

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/01/005426
Enrollment
120
Registered
2015-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Psoriasis

Interventions

Intervention1: Group - A: Panchatikta guggulu Ghrita and Brihanmarichadya Taila.: Group - A: i) Panchtiktaguggulu Ghrita (AFI-Part-I, vol.-I, 6:27, Page-121)(API Part II,Vol.II p.no.121-123)) Dose: 6

Sponsors

Central Council for Research in Ayurvedic Sciences CCRAS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex with age between 18 and 60 years. 2. Known cases of psoriasis, without psoriatic arthropathy, Exhibiting psoriatic triad â?? a. Bright pink or red lesions with pronounced edges, covered with silvery white scales, the scales can be easily separated from the lesion. b. Under the scales there appears a pinkish moist tender skin. c. With the scraping of the moist skin there appear tiny blood droplets (Auspitzâ??s sign) 3. Patients suffering from psoriasis with less than 50 % of the body surface involvement. 4. Disease duration between 3 months to 5 years. 5. V.D.R.L. / HIV/Hepatitis negative. 6. Positive histopathological finding.(Skin-biopsy) 7. Willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Generalized skin lesions, Herpes simplex, Herpes zoster, Scabies, Acne, Urticaria, Immunological medicated skin diseases like Pempigus vulgaris, Dermatitis ,herpetiformis, Guttate, Pustular, Lupus erythematous, Psoriatic arthropathy etc. 2. Patients with poorly controlled Hypertension (Blood pressure more than 160/100mm of Hg). 3. Pregnant or lactating women. 4. Patient with uncontrolled Diabetes Mellitus (Blood sugar fasting more than 250 mg/dl). 5. Patient suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Tuberculosis, Psycho â?? Neuro - endocrinal disorders, etc.). 6. Patientâ??s suffering/Past history of Heart disease, serious hepatic disorders, Severe Pulmonary Dysfunction, Renal Disorders etc. 7. Patients on medication with corticosteroids, phototherapy, biologics, antidepressants any other drugs that may have an influence on the outcome of the study. 8. Patients with concurrent serious hepatic disorder or renal disorders, AIDS, STD etc. 9. Alcoholics and/or drug abusers. 10. H/o hypersensitivity to the trial drug or any of its ingredients. 11. Patients who have completed participation in any other clinical trial during the past six months. 12. Any other condition which the Investigator thinks may jeopardize the study.

Design outcomes

Primary

MeasureTime frame
â?¢ Changes in Psoriasis Severity score.Timepoint: Two Years

Secondary

MeasureTime frame
â?¢ Changes in the clinical Sign & symptoms of Psoriasis. â?¢ Change in Dermatology life Quality Index (DLQI) Questionnaire. Timepoint: Two Years

Countries

India

Contacts

Public ContactDr Om Prakash

National Research Institute for Ayurveda - Siddha Human Resource Development

oprakash749@gmail.com9406581637

Outcome results

None listed

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