Skip to content

Chincha Bhallataka Vati for hypothyroidism

Role of Chincha Bhallataka Vati in the treatment of Primary Adult Hypothyroidism - A Standard Controlled Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/011039
Enrollment
30
Registered
2017-12-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Primary Adult Hypothyroidism

Interventions

Intervention1: chincha bhallataka vati: chincha bhallataka vati will be given in Primary adult hypothyroidism patients dose 2 tab(250mg)tds with luke warm water before mealfor 8 weeks. Control Interve

Sponsors

IPGT and RA Gujrat ayurved university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients having clinical features of Hypothyroidism 2 S.TSH level above 4.25mIU/mL 3 Age 20-60 years of either sex and willing to give their consent to participate in the study 4 Patient eligible for Koshtha Shuddhi

Exclusion criteria

Exclusion criteria: 1 Patients Suffering from Ischemic heart diseases, Uncontrolled hypertension, Myocardial Infarction, Cerebrovascular event, Cardiac arrhythmias, Pregnancy lactating mother, Active malignant disease 2 Chronicity more than 10 year 3 Secondary Hypothyroidism, Hashimoto thyroiditis, peptic ulcer, Acute illness like infection, Psychosis or patient having history of Hyperacidity, or pre-dominant Pitta Prakriti or bleeding disorder 4 Patient age below 20 year and above 60 year of either sex. 5 Patients not eligible for Koshtha Shuddhi

Design outcomes

Primary

MeasureTime frame
Efficacy,Control of hypothyroidism symptoms.Timepoint: 2 months

Secondary

MeasureTime frame
efficacyTimepoint: 2 months

Countries

India

Contacts

Public ContactDr Charu Roat

ipgt and ra gujarat ayurved university jamnagar

kaurmandip22@yahoo.com9427572306

Outcome results

None listed

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