- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05604664
Clinical Value and Efficacy Index of Lymphadenectomy for Thoracic Escc
November 3, 2022 updated by: Yongtao Han
Clinical Value and Efficacy Index of Lymphadenectomy for Thoracic Esophageal Squamous Cell Carcinoma
The goal of this observational study is to to clarify the focus of lymph node dissection during esophagectomy.. The main question[s] it aims to answer is:
- provide a basis for accurate staging and the relationship between OS and lymph node dissection
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
1727
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sichuan
-
Chengdu, Sichuan, China, 610041
- Sichuan Cancer Hospital and Research Institute
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
(1) Pathologic findings proved esophageal cancer (8th AJCC/UICC stage T1b-4aN0-3M0).
(2) underwent esophagecomy (two-field or three-field LN dissection).
(3)The primary tumor was thoracic esophageal cancer.
Description
Inclusion Criteria:
- Pathologic findings proved ESCC (8th AJCC/UICC stage T1b-4aN0-3M0)
- Underwent esophagecomy (two-field or three-field LN dissection)
- The primary tumor was thoracic ESCC
Exclusion Criteria:
- Located outside the thoracic
- Patients underwent salvage or R1/R2 esophagecomy
- The number of resected lymph nodes (RLNs) less than 15
- With neoadjuvant therapy(NT) or salvage chemoradiotherapy(SCRT)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
5-year survival rate of lymph nodes metastases (%) in patients
Time Frame: 2010.1.1-2017.12.30
|
Surgical data were retrospectively collected
|
2010.1.1-2017.12.30
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2022
Primary Completion (Actual)
October 1, 2022
Study Completion (Actual)
October 10, 2022
Study Registration Dates
First Submitted
October 29, 2022
First Submitted That Met QC Criteria
November 2, 2022
First Posted (Actual)
November 3, 2022
Study Record Updates
Last Update Posted (Actual)
November 4, 2022
Last Update Submitted That Met QC Criteria
November 3, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- SCCH-TS2203
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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