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Evaluation of the effect of Virechan and Shilajit in comparision to Thyroxine Sodium in the management of Hypothyroidism

Evaluation of the effect of Virechan and Shilajit in comparision to Thyroxine Sodium in the management of Hypothyroidism. - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/062170
Enrollment
40
Registered
2024-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: E039- Hypothyroidism, unspecified

Interventions

None listed

Sponsors

Pt Khushilal Sharma Govt (Autonomous) Ayurveda College and Institute Bhopal (MP)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Newly diagnosed case of Hypothyroidism. Patients age between 25 years to 45 years. Patients those fit for Virechan Karma.

Exclusion criteria

Exclusion criteria: All complicated cases of Hypothyroidism, myxedema, severe mental illness, thyroid cancer etc. and other disease associated with endocrine imbalance. Patients having chronic systemic illness. Congenital hypothyroidism Pregnant women and Lactating Mother. Patients having undergone thyroid surgery. Patients those unfit for Virechan Karma.

Design outcomes

Primary

MeasureTime frame
It is expected that at the end of the study we would be able to demonstrate the effects of virechan karma and shudhh shilajit in the management of hypothyroidism. It is further expected that this study would be able to provide comparative efficacy between the trialed treatment to that of standard controle ie. Thyroxine sodium.Timepoint: 45 Days

Secondary

MeasureTime frame
Thyroxin Sodium is more effective than Virechana Karma And Shuddha ShilajitTimepoint: 45 Days

Countries

India

Contacts

Public ContactDr Sonika Solanki

Pandit Khushilal Sharma Government Ayurveda college and Institute Bhopal

preetichaturvedi227@gmail.com7999013557

Outcome results

None listed

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