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To compare the effect of Vamanakarma followed by shunthi churna in one group of 15 patients and only shunthi churna without Vamanakarma in other group of 15 patients of hypothyroidism wsr to Agnimandya.

A Comparative study on the efficacy of Shunthi Churna with and without Vamana Karma in the management of Hypothyroidism wsr to Agnimandya. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067233
Enrollment
30
Registered
2024-05-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: E038- Other specified hypothyroidism

Interventions

None listed

Sponsors

Nidhi Kumari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Vamana yogya 2.person between the age group of 20-60 years 3.diagnosed cases of Hypothyroidism (primary and subclinical)on the basis of Sr. TSH, Sr. T3,Sr. T4 4.patients with clinical sign and symptoms of hypothyroidism

Exclusion criteria

Exclusion criteria: 1.Vamana Ayogya 2.Patients with HTN, Asthma, Cardiac disease, diabetes, pregnancy and other systemic disorders which may lead the patient to fatal condition during the VamanaKarma 3.Patients with congenital and Secondary Hypothyroidism 4.If Serum TSH level more than 100mIU/L were excluded 5.chronicity of hypothyroidism more than 5years

Design outcomes

Primary

MeasureTime frame
Sign and symptoms will be assessed before and after treatment . Those are puffiness over face and eyelids, oedema, dry and coarse skin,breathlessness, constipation, weakness,lethargy,fatigue,muscle ache,duration of menstrual blood, interval between two menstrual cycles and hairfallTimepoint: Group A 45 days Group B 28 days

Secondary

MeasureTime frame
Thyroid profile test investigations will be done in patients before and after treatment. Increased Serum TSH level is the key marker of hypothyroidism and changes in its level is to be assessedTimepoint: Group A 45 days Group B 28 days

Countries

India

Contacts

Public ContactDr. Akhilesh Prasad Singh

Government Ayurvedic College and Hospital

drapsinghpatna@gmail.com8002680973

Outcome results

None listed

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