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To study the efficacy of an Indigenous Herbal Combination as an externalApplication in Skin itching, scaling, hyperpigmentation, discoloration, cracks & dryness

Phase 2
Conditions
Health Condition 1: L99- Other disorders of skin and subcutaneous tissue in diseases classified elsewhere
Registration Number
CTRI/2023/09/057534
Lead Sponsor
Supreem Pharmaceuticals Private Limited Mysuru
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Subjects age group between 18- 60 years, irrespective of gender.

2.Subjects even with chronic skin lesion under medication (oral & Topical Applications).

3. Different skin symptoms such as Scaling, Discoloration, Cracks in the Skin, Dryness in the Skin, Itching, Hyperpigmentation

Exclusion Criteria

Skin Conditions with open cuts, Wound & Burns

• Excessive serous and pus discharge.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
reduction in itching , discoloration.Timepoint: 15 days
Secondary Outcome Measures
NameTimeMethod
reduction in all symptoms & signs of skin lesionsTimepoint: 30days
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