The Importance of Thymus Anatomy to the Radical Resection of Thyroid Cancer Surgery and the Protection of Parathyroid Function
NCT ID: NCT06851260
Last Updated: 2025-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
5 participants
INTERVENTIONAL
2025-02-20
2026-03-30
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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thymus anatomy
Fine dissection and preservation of thymus tissue are required during surgery.
Fine-dissection of the thymus
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.
non-thymus anatomy
Conventional surgical method for central lymph node dissection
No interventions assigned to this group
Interventions
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Fine-dissection of the thymus
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.
Eligibility Criteria
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Inclusion Criteria
* 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:
Exclusion Criteria
* 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.
ALL
No
Sponsors
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Tianjin Medical University Cancer Institute and Hospital
OTHER
Responsible Party
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Other Identifiers
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E20241348
Identifier Type: -
Identifier Source: org_study_id
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