A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF BRIHTYADI LEPA(Chakradatta)AND RAKTAMOKSHANA BY GHATI YANTRA IN CASES OF Hair fall

Phase 2

Completed

• Conditions: Health Condition 1: -

• Registration Number: CTRI/2021/05/033343
• Lead Sponsor: State Ayurveda College and Hospital Lucknow

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-05-20
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

A-SUBJECTIVE PARAMETERS-

1Patients who give the consent to participate in clinical trial.

2Patients of age group 21-40 years.

Essential Criteriaââ?¬â??Gradual hair fall, more than 100 hairs par day in a couple of weeks.For males, the pattern typically involves loss of the frontal hairline with hair loss at the vertex (or top of the scalp) and progress over time. For females, the pattern is more variable, but most often spares the frontal hairline and involves diffuse thinning of hair over the crown of the scalp, sparing the back. This again progress over time.

Non-Essential/Others Criteria

a.Darunaka (Dandruff)

b.ShirahKandu (Itching on scalp)

c.Kesh Tanutva (Thinning of Hairs)

d.Kesh Rukshta (Dryness of Hair)

e.Kesh Bhoomi Sweda (Sweating on Scalp)

B-OBJECTIVE PARAMETERS

a. Total Number of hair loss/day

b.After sleep numbers of hairs on Pillow

c.During hair wash number of hairs

d.During combing hair number of hairs

e.Hair pull test

f.Hormone test -testosterone

Patients having Essential criteria along with minimum 50% of Non-essential parameter will be registered for clinical trial.

Exclusion Criteria

1Cases of any chronic systemic disorders

2Thyroid disorder

3Traumatic hair loss

4Burns,

5 chemotherapy

6Bacterial Infection

7Localized surgery

8Cases with family history of Alopecia.

9More than 75% hair loss.

10Age below 21 year & above 40 year

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1To evaluate clinical efficacy of Brihatyadilepa in Khalitya. <br/ ><br>2To evaluate clinical efficacy of Raktamokshna by Ghati-Yantra in Khalitya. <br/ ><br>3Comparative efficacy between Lepan Karma and Raktmokshna. <br/ ><br>4To evaluate cumulative effect of Lepa & Raktamokshna <br/ ><br>Timepoint: 3 months <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
1To assess the adverse effect of drug if any. <br/ ><br>2To provide scientifically proved,effective management in Khalitya <br/ ><br>Timepoint: 3 Months