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Studying antithyroglobulin antibodies in hashimotos disease with murphy repertory

Not Applicable
Conditions
Health Condition 1: E063- Autoimmune thyroiditis
Registration Number
CTRI/2024/03/063729
Lead Sponsor
il
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients suffering from Hashimoto’s thyroiditis with elevated TSH, anti-Thyroglobulin Ab.

Female patients will be included.

Patients between 18-60 years of age.

Exclusion Criteria

Pregnant, post-partum and nursing women will be excluded.

Known cases of other autoimmune disorders.

Known cases of thyroid malignancy.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The efficacy of Homoeopathic medicines in reducing the Anti-thyroglobulin antibody level in Hashimoto’s thyroiditis will be proved before and after an interval of 6 months of the treatment. <br/ ><br>Cases will be evaluated for age, sex, occupation, symptoms presented, values of anti-thyroglobulin antibody (anti-Tg), thyroid peroxidase antibodies and TSH will be considered for statistical analysis and to derive the result, thereby validating the study.Timepoint: The efficacy of Homoeopathic medicines in reducing the Anti-thyroglobulin antibody level in Hashimoto’s thyroiditis will be proved before and after an interval of 6 months of the treatment. <br/ ><br>Cases will be evaluated for age, sex, occupation, symptoms presented, values of anti-thyroglobulin antibody (anti-Tg), thyroid peroxidase antibodies and TSH will be considered for statistical analysis and to derive the result, thereby validating the study.
Secondary Outcome Measures
NameTimeMethod
The symptomatic improvement of the patient with hypothyroidism assessed by Zulewski clinical score will reveal the efficacy of Murphy repertory in the treatment of Hashimoto’s thyroiditis. <br/ ><br>An alphabetical repertory will be constructed on thyroid disorders.Timepoint: Medicines given will be observed for 2 weeks consecutively for 6 months
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