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Clinical Trials/CTRI/2025/02/080163
CTRI/2025/02/080163Not yet recruitingNot Applicable

A CLINICO-COMPARATIVE STUDY OF KAISORA GUGGULU WITH MANJISTHADI KVATHA AND EKAVINSATIKO GUGGULU WITH NISADI KVATHA IN THE MANAGEMENT OF PSORIASIS

J S Ayurveda Mahavidyalaya1 site in 1 country40 target enrollmentStarted: February 20, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
To observe and find out changes in signs and symptoms of psoriasis after the oral administration of above mentioned medicinnes

Study Overview

Brief Summary

Psoriasis is a complex, chronic, multifactorial, inflammatory disease that

involves hyper proliferation of keratinocytes in the epidermis, with an

increase in the epidermal cell turnover rate. 20 patient of psoriasis who

fulfill the inclusion criteria will be selected from opd and give them oral

administration of khadirastak kwatha 40 ml twice a day and manjisthadi

taila for local application twice a day. Patient will be treated for 8 weeks.

Patients will be assessed before and after the treatment.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
16.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Who fulfilled the diagnostic criteria mentioned as sign and symptom Any three of these symptoms 1.Scaling 2.Itching (Kandu) 3.Erythema 4.Loss of perspiration 5.Dryness Any one of these signs 1.Auspitz sign 2.Candle grease sign 3.Koebners phenomenon Patients of age between 18 to 60 years and of both genders.

Exclusion Criteria

  • Pregnant or lactating females.
  • 1.Known cases of diseases like AIDS, STD, TB, heart diseases and other disorders that lead to fetal conditions for the patients.
  • 2.Patients having diabetes mellitus.
  • 3.Other concomitant skin diseases occurring with the allergic reaction of any other disease.

Outcomes

Primary Outcomes

To observe and find out changes in signs and symptoms of psoriasis after the oral administration of above mentioned medicinnes

Time Frame: A patient will be treated at O.P.D. level for 8 weeks of treatment. They will be instructed to visit the hospital every 2 weeks at intervals.

Secondary Outcomes

  • To evaluate the changes in the PASI index in the patients of psoriasis.(2.To find out the improvement in quality of life through changes in DLQI in the patients of psoriasis.)

Investigators

Sponsor
J S Ayurveda Mahavidyalaya
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr Manali Chauhan

J.S Ayurveda

Study Sites (1)

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