NCT06851260

Brief Summary

Thyroid cancer is one of the most common endocrine malignancies. In the past three decades, the incidence rate of thyroid cancer has continued to rise rapidly in many countries and regions around the world. The incidence rate of thyroid cancer in China is increasing year by year. The standardized incidence rate increased from 1.4/100000 person years in 1990 to 14.65/100000 person years in 2016. It has become the seventh malignant tumor in China with incidence rate, especially the incidence rate of women. Although differentiated thyroid cancer (DTC) has a low degree of malignancy, it still poses a threat to the life, health, and quality of life of patients. Due to its low mortality rate and long survival period, standardized diagnosis, treatment, and follow-up are even more necessary. The 5-year survival rate of thyroid cancer in China has increased significantly from 67.5% in 2003-2005 to 84.3% in 2012-2015, but still lags far behind the 98.3% in the United States. The current treatment for thyroid cancer is mainly surgical treatment. The development concept of tumor surgery is first radical, followed by functional preservation, and finally aesthetic incision. Standardized and thorough radical surgery is the most critical link to improve patient prognosis and reduce the occurrence of complications. Lymph node metastasis is a common cause of patient recurrence. According to literature reports, the central lymph node metastasis rate after DTC surgery is 24% -64%, which affects the prognosis and quality of life of patients, often requiring secondary surgery, increasing the incidence of postoperative complications and patient burden. Therefore, thyroid cancer surgery requires standardized and thorough neck lymph node dissection. Based on surgical experience and autopsy research, several pre tracheal lymph nodes are often hidden in the deep surface of the thymus from the inferior pole of the thyroid to the upper edge of the unnamed artery. Postoperative recurrence of central lymph nodes often occurs in this area. Therefore, during the initial surgery, the neck segment of the thymus must be freed and pulled away to the shallow layer to thoroughly clean the pre tracheal lymph nodes hidden in the deep surface of the thymus. A considerable number of zone VII lymph nodes can also be pulled out to make the central lymph node cleaning more thorough. However, current surgical standards and guidelines do not emphasize the importance of thymus anatomy.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
5

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 20, 2025

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

February 24, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 28, 2025

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2026

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2026

Completed
Last Updated

February 28, 2025

Status Verified

February 1, 2025

Enrollment Period

1.1 years

First QC Date

February 24, 2025

Last Update Submit

February 24, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • The effectiveness of surgery

    Count the number of central lymph node dissection and positive lymph nodes in routine pathological examination after surgery. Follow up neck ultrasound will be conducted at 3 months, 6 months, and 1 year after surgery, and then every 6 months.

    13 months

Secondary Outcomes (1)

  • the PTH level after surgery

    13 months

Other Outcomes (1)

  • Survival situation

    13 months

Study Arms (2)

thymus anatomy

EXPERIMENTAL

Fine dissection and preservation of thymus tissue are required during surgery.

Procedure: Fine-dissection of the thymus

non-thymus anatomy

NO INTERVENTION

Conventional surgical method for central lymph node dissection

Interventions

In thyroid surgery, precise dissection and preservation of thymus tissue are used to improve the protection of the lower parathyroid gland function and increase the curative effect of the surgery.

thymus anatomy

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patients diagnosed with thyroid cancer who require total thyroidectomy and bilateral central lymph node dissection.
  • The subjects voluntarily joined this study, signed an informed consent form, had good compliance, and cooperated with follow-up.
  • Age at the time of signing the informed consent form is between 18 and 80 years old, regardless of gender.
  • The physical fitness score of the Eastern Cooperative Oncology Group (ECOG) is 0 or 1.
  • Expected survival period is not less than 1 year.
  • Male and female patients of childbearing age agreed to use reliable methods of contraception before entering the trial, during the research process, and up to 8 weeks after discontinuation of medication.
  • Good organ function:

You may not qualify if:

  • There are locally advanced unresectable or metastatic diseases.
  • History of non infectious pneumonia/interstitial lung disease requiring steroid treatment, or current pneumonia/interstitial lung disease requiring steroid treatment.
  • Known history of active tuberculosis.
  • Known to have active infections that require systematic treatment.
  • Any subjects with known or suspected autoimmune diseases or immune deficiencies.
  • Uncontrolled active hepatitis B (defined as hepatitis B B virus surface antigen \[HBsAg\] test result in screening period is positive and HBV-DNA test value is higher than the upper limit of normal value in the laboratory department of the research center.
  • Subjects with HBV-DNA levels\<500 IU/mL within 28 days prior to randomization, who have received local standard antiviral treatment for at least 14 days and are willing to continue receiving antiviral treatment during the study period, are eligible for enrollment; Subjects with active hepatitis C (defined as those who test positive for hepatitis C virus surface antibody \[HCsAb\] and HCV-RNA during the screening period).
  • Known human immunodeficiency virus (HIV) infection (known to be HIV antibody positive).
  • Administer a live vaccine within 30 days prior to the first dose.
  • Have ≥ grade 2 peripheral neuropathy.
  • Has experienced severe allergic reactions to other monoclonal antibodies.
  • Known to have serious or uncontrolled underlying diseases; Including but not limited to hemodynamic instability cardiovascular events, symptomatic cerebrovascular events, and Child Pugh A or higher liver cirrhosis that occur within 6 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Thyroid Neoplasms

Condition Hierarchy (Ancestors)

Endocrine Gland NeoplasmsNeoplasms by SiteNeoplasmsHead and Neck NeoplasmsEndocrine System DiseasesThyroid Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 24, 2025

First Posted

February 28, 2025

Study Start

February 20, 2025

Primary Completion

March 20, 2026

Study Completion

March 30, 2026

Last Updated

February 28, 2025

Record last verified: 2025-02