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To study the effect of haritaki (terminalia chebula) in spring season as an adjuvant in health promotio

Phase 2
Registration Number
CTRI/2024/07/071653
Lead Sponsor
Dr Sushma T J
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1) Healthy volunteers of age group 20-40 years irrespective of genders.

2) Participants with bio chemical parameters in concern within normal range

3) Participants willing to give a written consent

Exclusion Criteria

1) Subjects with any systemic illness

2) Subjects contraindicated for Haritaki administration7

3) Pregnant and lactating women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improved Hb, TC, DC, ESRTimepoint: 40th day
Secondary Outcome Measures
NameTimeMethod
Maintenance of improved Hb, TC, DC, ESRTimepoint: 60th day
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