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Clinical Study on Xiaoyingsanjie External Prescription in Treatment of Hashimoto's Thyroiditis

Clinical Study on Xiaoyingsanjie External Prescription in Treatment of Hashimoto's Thyroiditis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053309
Enrollment
Unknown
Registered
2021-11-18
Start date
2021-11-18
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

Hashimoto's Thyroiditis

Interventions

Experimental group:External application of Xiao Ying San Jie Fang
Control group:Placebo

Sponsors

Dongfang Hospital Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with normal thyroid function who meet the diagnostic criteria of Hashimoto's thyroiditis in western medicine; 2. Accords with TCM syndrome differentiation and belongs to qi stagnation and phlegm obstruction syndrome; 3. Aged 18-70 years; 4. Participated in this study voluntarily, with good compliance and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have recently taken traditional Chinese medicine preparations for treating thyroiditis of qi stagnation and phlegm stagnation type; 2. Pregnant or lactating women; 3. Patients with serious primary diseases and mental diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic system; 4. Patients with thyroid cancer and unexplained fever; 5. Patients allergic to the experimental drug; 6. Patients who have participated in clinical trials of other drugs in recent 3 months.

Design outcomes

Primary

MeasureTime frame
Total effective rate of efficacy;

Secondary

MeasureTime frame
TCM symptom score;TG-Ab, TPO-Ab;

Countries

China

Contacts

Public ContactHu Hao

Dongfang Hospital Beijing University of Chinese Medicine

457582239@qq.com+86 13811304720

Outcome results

None listed

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