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The clinical application of ultrasound-guided Mitoxantrone Hydrochloride Injection for Tracing in the localization of lateral cervical lymph nodes in thyroid cancer

The clinical application of ultrasound-guided Mitoxantrone Hydrochloride Injection for Tracing in the localization of lateral cervical lymph nodes in thyroid cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113161
Enrollment
Unknown
Registered
2025-11-25
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Papillary thyroid carcinoma

Interventions

Trial Group:Mitoxantrone hydrochloride injection for tracing was used for preoperative localization under ultrasound guidance

Sponsors

Hunan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age of 18-70 years old (including 18 and 70 years old), male and female; 2. Preoperative clinical diagnosis of PTC, imaging examination (such as ultrasound, CT) suspected lateral cervical lymph node metastasis, after MDT discussion, lateral cervical lymph node dissection was planned; 3. No obvious contraindications to surgery were found in routine preoperative examination; 4. Be able to communicate well with researchers and complete research according to research regulations; 5. Patients voluntarily participated in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with hypersensitivity constitution, or history of severe drug allergy, or allergy to anthraquinone drugs; 2. History of drug abuse or substance abuse within the past year; 3. History of thyroid surgery, radioactive iodine therapy, or neck radiotherapy; 4. Hemoglobin (HB) 3 times the upper limit of normal (in patients with liver metastasis, ALT and AST >5 times the upper limit of normal); 6. Serum creatinine (Cr) >1.5 times the upper limit of normal; 7. Participation in other clinical trials within 3 months prior to this trial; 8. Patients with neurological disorders, psychiatric disorders, or intellectual disabilities who are unable to accurately describe their own symptoms; 9. Pregnant or lactating women; 10. Subjects and their spouses have plans for pregnancy during the trial period or within 6 months after the trial; 11. Researchers involved in this trial shall not participate as subjects; 12. Other subjects deemed unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
The identification rate and the number of lymph nodes dissected marked by lymphatic tracer;Evaluation of the diagnostic efficacy of preoperative auxiliary examination methods;

Secondary

MeasureTime frame
Postoperative recurrence rate;Postoperative complication rate;Surgical duration and extent of lymph node dissection;

Countries

China

Contacts

Public ContactPeng Xiaowei

Hunan Cancer Hospital

pengxiaowei@hnca.org.cn+86 731 88651812

Outcome results

None listed

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