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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05274464
Other study ID # HAS-GC-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2004
Est. completion date December 31, 2019

Study information

Verified date March 2022
Source Fujian Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to develop a nomogram to predict postoperative recurrence of HAS and guide individually tailored surveillance strategies.


Description:

Patients were included from the China Hepatoid Adenocarcinoma of the Stomach Study Group (China-HASSG) database, which comprises 14 tertiary referral centers. All the patients who had undergone complete resection of a primary HAS between April 2004 and December 2019 were included. First, univariate analysis was performed in Cox regression to identify the risk factors associated with RFS. Next, variables with P< 0.05 in univariable analysis were included in the multivariable model, and the forward likelihood ratio method was used for analysis to confirm the independent prognostic factors associated with RFS. Finally, based on the results of multivariable analysis, variables that achieved significance at P< 0.05 were selected to formulate a nomogram.


Recruitment information / eligibility

Status Completed
Enrollment 261
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients who had undergone complete resection of a primary HAS between April 2004 and December 2019 Exclusion Criteria: - Patients with metastatic disease, patients who had undergone palliative surgery, patients who had died within 30 days, and patients who were lost to follow-up

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Fujian Medical University Union Hospital Fuzhou Fujian

Sponsors (1)

Lead Sponsor Collaborator
Fujian Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reurrence-free survival Reurrence-free survival was defined as the time interval from the date of the operation to the date of first recurrence or death from any cause. 3 year
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