A Randomised Comparative Clinical Study To Evaluate The Efficacy Of Drug With and Without Yoga In Cases Of Hypothyroidism.

A Randomised Comparative Clinical Study To Evaluate The Efficacy Of Gomutra Bhavit Jalkumbhi Bhasma And KPG Vati With And Without Ujjayi Pranayama In Cases Of Hypothyroidism.

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/09/045491

Enrollment

Registered

2022-09-13

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

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

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who are freshly diagnosed or mild cases of Hypothyroidism with increased TSH level(TSH level between > 4.5-12.5 microIU/ml 2. Patients who are ready to switch over to Ayurvedic medicine and have signed the consent form. 3. 4 out of 6 major symptoms and minor symptoms may or may not be signed the consent form. 4. Patients with hypothyroidism who are interested in involving themselves in pranayama practice with drugs treatment.

Exclusion criteria

Exclusion criteria: 1.TSH level above 12.5 microIU/ml. 2. Patients who have under gone any type of thyroid surgery and recent abdominal or spinal surgery. 3. patients whose symptoms are worsely aggravated after leaving the modern drug Levo-thyroxine( in the washout period). 4. Hyperthyroidism, Neoplasia, toxic goiter are excluded.. 5. Patients suffering from congenital hypothyroidism. 6 Obese female with pregnancy or lactation and children.

Design outcomes

Primary

Measure	Time frame
Clinical outcome assessment among the people registered under the study will be done through - Increased level of TSH above (4.5microIU/ml),weight gain, oedema, Hoarseness of voice ,constipation,Generalized pain etc all signs symptoms are graded 0,1,2,3 on the basis of intensity confirmed by clinical examination before trial.The clinical improvement during and after trial will also be correlated and assess with previous grading.Timepoint: 90 days	—

Measure

Time frame

Clinical outcome assessment among the people registered under the study will be done through - Increased level of TSH above (4.5microIU/ml),weight gain, oedema, Hoarseness of voice ,constipation,Generalized pain etc all signs symptoms are graded 0,1,2,3 on the basis of intensity confirmed by clinical examination before trial.The clinical improvement during and after trial will also be correlated and assess with previous grading.Timepoint: 90 days

—

Secondary

Measure	Time frame
Quality of life improvement.Timepoint: 90 days	—

Countries

India

Contacts

Public ContactDr Jyoti

State Ayurvedic College and Hospital

anant10patel@gmail.com9452274856

Outcome results