Skip to content

Ayurvedic Treatment Package in Plaque Psoriasis

A Randomized Open Label Clinical Trial on the Efficacy of an Ayurvedic Treatment Package on Symptom Severity and Quality of Life in Plaque Psoriasis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04146558
Enrollment
90
Registered
2019-10-31
Start date
2019-12-04
Completion date
2023-12-31
Last updated
2025-06-15

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

Conditions

Psoriasis

Brief summary

Psoriasis is a chronic, immune-mediated inflammatory skin disease that is associated with substantial impairment of physical and psychological quality of life. The conventional treatment protocols manages the condition but with remissions and relapses which create anxiety in patients. Many of the patients withdraw from active social life as the disease attains chronicity. Several studies are pointing towards a conjoint management strategy incorporating the traditional and alternate medical systems. In this regard, Ayurveda is commonly used by psoriatic patients in India. Considering this fact it is high time to conduct a study to scientifically evaluate the efficacy of Ayurvedic treatment protocol in managing psoriasis as well as its potential to improve the quality of life.

Interventions

DRUGIndividualized internal ayurvedic treatment

All possible internal preparations will be administered for a period of 12 months. All administered preparations with its dosage and duration will be documented All preparations will be subjected to lab test for clearing heavy metal and pesticide content before the administration

OTHERExternal ayurvedic treatment

Application of warm external oil (Ayyapala kera tailam) on affected parts twice daily

Sponsors

Poomulli Neelakandan Namboodiripad Memorial Ayurveda Medical College
CollaboratorUNKNOWN
Universität Duisburg-Essen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with psoriasis having age 18 years or more * Patients with moderate-to-severe plaque psoriasis with a PASI score of 12 or higher * Psoriasis diagnosed 6 months or more before study entry * Those who are poorly controlled based on physicians assessment with topical treatments, phototherapy, systemic therapy, or a combination of these therapies. * Participants who have given informed consent.

Exclusion criteria

* Participants with other systemic illnesses * Lactating and pregnant mothers. * Alcohol dependence/Narcotic dependence /Steroid dependence * In the judgment of the investigator, unable or unwilling to follow the protocol and instructions

Design outcomes

Primary

MeasureTime frameDescription
Psoriasis-specific quality of life6 monthsPsoriasis specific DLQI scores

Secondary

MeasureTime frameDescription
Psoriasis Severity3 monthsPsoriasis Area Severity Index (PASI) score
Psoriasis-specific quality of life3 monthsPsoriasis specific DLQI scores
Adverse events3 months

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026