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Central Cervical Dissection for Clinical Node Negative Papillary Thyroid Carcinoma

Zhejiang University logo

Zhejiang University

Status

Not yet enrolling

Conditions

Lymph Node Metastases

Treatments

Procedure: lymph node dissection

Study type

Interventional

Funder types

Other

Identifiers

NCT03813173
ZhejiangU20190116

Details and patient eligibility

About

This study is divided into three stages. In the first stage, the investigators try to explore the objective clinical imaging standard of cN0PTC on the basis of previous studies, formulate the "clinical imaging standard of cN0PTC", and randomly enroll 2000 patients under the premise of meeting the standard to establish the "predictive model of cN0-pN+PTC".

In the second stage, 2000 patients will be enrolled to test and improve the evaluation efficiency of "cN0-pN+PTC prediction model".

In the third stage, 2 000 patients without lymph node metastasis assessed by "cNo-pN+ PTC prediction model" will be randomly divided into experimental group and control group. The experimental group will be treated with pCND, while the experimental group will be treated without pCND. The central lymph node metastasis probability, the number and size of metastatic lymph nodes in the control group will be observed after operation. The two groups will be followed up for 5, 10, 15 and 20 years to observe the RFS and OS, so as to further evaluate the "cN0-pN+PTC prediction model" scientifically.

Enrollment

6,000 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Phase I and II:

    1. aged 18 to 80 years old;
    2. the primary treatment of patients with unilateral or bilateral PTC;
    3. ultrasound showed that the tumor was localized in the thyroid gland, and the maximum diameter of each lesion was less than 4cm;
    4. ultrasonography of cervical VI lymph nodes: the shortest diameter < 4 mm, no calcification, no cystic change, no local or global echo enhancement;
    5. CT scan of cervical VI lymph nodes: the shortest diameter < 4 mm, no calcification, no cystic change, no enhancement (CT value 40HU or not higher than banded muscle level), no cluster distribution;
    6. patients will voluntarily enter the study after informed consent;

Phase III:

  1. aged from 18 to 80 years old;
  2. ultrasound showed that the tumor was localized in the thyroid gland, and the maximum diameter of each lesion was less than 4cm;
  3. Unilateral or bilateral PTC without lymph node metastasis assessed by "cNo-pN+ PTC prediction model";
  4. patients will voluntarily enter the study after informed consent.

Exclusion criteria

  • (1) patients refused to participate in the study; (2) non first operation patients; (3) Lateral cervical lymph nodes or distant metastasis; (4) Hashimoto's disease; (5) history of neck trauma.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

6,000 participants in 2 patient groups

central cervical dissection
Active Comparator group
Treatment:
Procedure: lymph node dissection
non central cervical dissection
Experimental group
Treatment:
Procedure: lymph node dissection

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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