ROLE OF GUDUCHI(PROCESSED) ON EKA KUSTHA (PSORIASIS)

Phase 2

Not yet recruiting

• Conditions: Patients having signs and symptoms of EKA KUSTHA (Psoriasis)

• Registration Number: CTRI/2013/12/004213
• Lead Sponsor: Institute for Post Graduate Teaching and Research in Ayurveda

Brief Summary

The present study is designed with the aim to evaluate the efficacy of *Swarasa* *bhavita Guduchi Churna* (powder of Guduchi levigated with its juice) derived by more duration of immersion (12 hrs) is more effective as compared to the sample derived by less duration of immersion (extracted immediately).

Study will be double blind, randomized trial. Selected patients will be studied under following groups:

 

| | | | | |

| --- | --- | --- | --- | --- |

|**Grouping**

**Drug Formulation**

**Dosage (powder)**

**For local**

**Application**

**Duration**

|Group A

SBGC1- with less duration of immersion

6 gm per day in divided doses before meal.

Tila Taila Qs

8 weeks

|Group B

SBGC2- with more duration of immersion

6 gm per day in divided doses before meal.

Tila Taila Qs

8 weeks

**Follow up:**   Patients will be reviewed after each 7 day for a period of 4 weeks.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2013-12-12
• Study Start: 2013-12-20

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

•Patients having classical sign and symptoms of Eka Kustha •Age group of patients will be between 16-60 years.

Exclusion Criteria

• •Life threatening medical and surgical emergencies.
• •Age below 16 and above 60 years •Known case of D.M with uncontrolled blood sugar level, AIDS, Malignancy, Immuno-compromised state etc.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
•The obtained data will be statistically analyzed and presented along with explanatory notes, discussion and conclusion.	30 days
•Improvement in the signs and symptoms of the disease as per Ayurvedic texts.	30 days

Secondary Outcome Measures

Name	Time	Method
Improvement will be assessed on the basis of relief found in cardinal symptoms of disease Progress in the signs and symptoms based on the standard pattern will be applied before and after treatment.	30 days

Trial Locations

Locations (1)

Institute for Post Graduate Training and Research in Ayurved; 🇮🇳 Jamnagar, GUJARAT, India

Institute for Post Graduate Training and Research in Ayurved

🇮🇳Jamnagar, GUJARAT, India

SANDEEP AGRAWAL

Principal investigator

9998823095

drsandeep.ayu88@gmail.com