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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04820712
Other study ID # FirstAHGTCMU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2020
Est. completion date January 1, 2021

Study information

Verified date March 2021
Source The First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study utilizes a new method to explore compare the overall survival (OS) and cancer-specific survival (CSS) in patients aged 18-45 years with stage I-II HCC who underwent different types of surgery. The SEER database, which is one of the most comprehensive and authoritative databases concerning cancer, was used to estimate the survival benefit of patients who underwent local tumor destruction (LTD), wedge or segmental resection (WSR), lobectomy resection (LR), liver transplantation (LT), or non-surgery. This study discovered surgery offered a survival benefit compared with non-surgery for young patients with stage I-II HCC. Furtherly, LT is associated with superior survival than WSR, LR and LTD in those patients. Our results facilitate the selection of surgical strategies.


Description:

The SEER data contain no identifiers and are publicly available for studies of cancer-based epidemiology and survival analysis. Therefore, the current study was deemed to be exempt from Institutional Review Board approval and the need for informed consent was waived. The submitted magazine requires registration on the website, so this operation is needed.


Recruitment information / eligibility

Status Completed
Enrollment 664
Est. completion date January 1, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: 1. Patients were diagnosed with colorectal cancer only; 2. Patients with simultaneous metastasis of liver and lung cancer cells; 3. Patients without metastasis resection; 4. whether they underwent palliative primary tumor resection was known; 5. Their cause of death was known; 6. Their survival time were known and greater than 0 month; 7. Patients were diagnosed with microscopic confirmation. Exclusion Criteria: - No

Study Design


Locations

Country Name City State
China linzhu Zhai Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Linzhu Zhai

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival Overall survival was defined as the duration between the surgery and death or the last follow-up 2004.1.1-2013.12.31
Secondary Cancer-specific survival Cancer-specific survival was defined as the period between the surgery and death due to cancer to reduce the impact of life-threatening comorbidities. 2004.1.1-2013.12.31
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