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Moxibustion aids in the implementation of active surveillance for papillary thyroid micro-carcinoma: study protocol for a non-randomized controlled trial

Moxibustion aids in the implementation of active surveillance for papillary thyroid micro-carcinoma: study protocol for a non-randomized controlled trial - Moxibustion aids in the implementation of active surveillance for papillary thyroid micro-carcinoma: study protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089377
Enrollment
Unknown
Registered
2024-09-06
Start date
2024-09-10
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Thyroid papillary microcarcinoma

Interventions

Active surveillance group(AS):Patients have regular follow-up appointments, and if the condition worsens or if the patient desires, surgery can be performed.
moxibustion+ AS group:Besides active surveillance, patients will receive moxibustion therapy twice a week for 10 minutes each site, over a period of 8 consecutive weeks, administered by the same thera

Sponsors

Affiliated Hospital of Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18-55 years old; 2. Ultrsound test confirms it to be non-invasive subtype of DTC; 3. The maximum diameter of the mass is less than 1cm, no evidence of extra-thyroidal invasion or distant metastasis; 4. The tumor locates far from important organs, such as the recurrent laryngeal nerve and trachea; 5. No history of thyroid surgery; 6. No history of malignant tumor; 7. Accept AS.

Exclusion criteria

Exclusion criteria: 1. With elevated thyroid-related antibody levels; 2. Hyporthyroidism or hyperthyroidism; 3. Patients are taking anti-thyroid medications or thyroid hormone replacement therapy; 4. With severe cardiovascular, liver, kidney or haematological diseases; 5. With mental disorders; 6. Pregnant or lactation 7. Afraid of moxibustion or having skin diseases at the moxibustion site

Design outcomes

Primary

MeasureTime frame
the percentage of patients who fullfil active surveillance;

Secondary

MeasureTime frame
the score of anxiety or depression;tumour growth or reduction;changes of the levels of TSH;

Countries

China

Contacts

Public ContactDongdong Chen

Affiliated Hospital of Jiangnan University

chendongdong1357@163.com+86 139 2112 4391

Outcome results

None listed

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