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

To evaluate the efficacy of ritu haritaki in vasanth ritu - An explorative preventive trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071653
Enrollment
60
Registered
2024-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Dr Sushma T J
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: 1) Subjects with any systemic illness 2) Subjects contraindicated for Haritaki administration7 3) Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
Improved Hb, TC, DC, ESRTimepoint: 40th day—

Secondary

MeasureTime frame
Maintenance of improved Hb, TC, DC, ESRTimepoint: 60th day—

Countries

India

Contacts

Public ContactDr P Sudhakar Reddy

JSS Ayurveda Medical College and Hospital

drpsreddy05@yahoo.com9916483919

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026