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Central cervical dissection for clinical node negative papillary thyroid carcinoma: a prospective study

Central cervical dissection for clinical node negative papillary thyroid carcinoma: a prospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019672
Enrollment
Unknown
Registered
2018-11-22
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-11-26

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

Conditions

Papillary thyroid carcinoma

Interventions

Experience group :non central cervical lymph node dissection
Control group:central cervical lymph node dissection

Sponsors

Affililated Hangzhou First People's Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

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 30 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

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.

Design outcomes

Primary

MeasureTime frame
recurrence;Lymph node metastasis;

Countries

China

Contacts

Public ContactLuo Dingcun

Affililated Hangzhou First People's Hospital, Zhejiang University School of Medicine

ldc365@163.com+86 13732225858

Outcome results

None listed

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