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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03161925
Other study ID # INW161116CLCS
Secondary ID
Status Active, not recruiting
Phase N/A
First received May 19, 2017
Last updated May 19, 2017
Start date November 28, 2016
Est. completion date August 31, 2017

Study information

Verified date May 2017
Source Beijing Insight Science & Technology Co. Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In order to make better use of clinical resources of the real world, strengthen the standardization of PLC diagnosis and treatment, and constantly improve the academic level of liver cancer in China, we intends to launch "Chinese Liver Cancer clinical Survey" project in cancer specialized hospitals and large general hospitals and to explore the best clinical pathway of PLC multidisciplinary consultation.


Description:

Primary liver cancer (PLC) is one of the most common malignant tumors of digestive system and also a serious threat to the health and safety of Chinese people, and has caused serious economic burden to the country. Research purposes: To understand the clinical characteristics of patients with primary liver cancer (PLC) in China; To investigate the etiology and pathogenesis of PLC in China; To understand the current status of clinical treatment of PLC in China, and to analyze the gaps among these conditions and domestic treatment guidelines, industry consensus, the international treatment guidelines; To understand the different treatment options and its clinical outcomes, and to explore the best treatment options; To explore the best clinical pathway of PLC multidisciplinary consultation; To provide the basis for the development of clinical guidelines for PLC in China.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 5000
Est. completion date August 31, 2017
Est. primary completion date August 31, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Diagnosis of PLC after January 1,2012;

- First treatment and efficacy evaluation.

Exclusion Criteria:

- Complicated with another primary malignant tumor and secondary liver cancer.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Beijing Insight Science & Technology Co. Ltd.

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival Overall survival 5 years
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