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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06165094
Other study ID # SCCH-TS2206
Secondary ID 2023YFQ0056
Status Completed
Phase
First received
Last updated
Start date January 1, 2009
Est. completion date December 1, 2023

Study information

Verified date December 2023
Source Sichuan Cancer Hospital and Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to learn about in health conditions of ESCC. The main question[s] it aims to answer are: •Lymph node metastasis(LNM) in cervical paraesophageal or supraclavicular which influence OS more. Participants will describe the main status quo after surgery Researchers will compare Lymph node metastasis(LNM) in cervical paraesophageal and supraclavicular to see if dead.


Description:

Demographic and pathologic data, including gender, age, pathological T stage, pathological N stage, 8th tumor-node-metastasis (TNM) stage, tumor location, tumor grade, lymphovascular invasion, perineural invasion, LNM, cervical paraesophageal LNM, supraclavicular LNM, and radical resection, were collected from the Sichuan Cancer Hospital and Institute Esophageal Cancer Case Management (SCH-ECCM) database.


Recruitment information / eligibility

Status Completed
Enrollment 122
Est. completion date December 1, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility The inclusion criteria were as follows: - patients who had undergone esophagectomy and - patients who exhibited LNM in the supraclavicular region. The exclusion criteria: - tumor location outside the thoracic region, - pathological examination results confirming the presence of non-squamous cell carcinoma, - patients with both cervical paraesophageal LNM and supraclavicular LNM, or - those with missing required data

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Sichaun cancer hospital Chengdu Sichuan

Sponsors (1)

Lead Sponsor Collaborator
Sichuan Cancer Hospital and Research Institute

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival OS was calculated from the month and year of surgery until the time of death or the last follow-up in March 2021. 2009.01.01-2017.12.30
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