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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01614548
Other study ID # ZZU2012
Secondary ID
Status Completed
Phase N/A
First received June 2, 2012
Last updated June 5, 2012
Start date January 2003
Est. completion date December 2011

Study information

Verified date June 2012
Source Zhengzhou University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Some recent reports indicate that incidence of prostate cancer is increasing rapidly in China. However, no large-scale survey of prostate cancer has been done in central China, few data are available regarding its management. The investigators aimed to analyze the management of prostate cancer and compare the outcome of patients with such a survey.

The investigators collected data of patients diagnosed with prostate cancer from the 2003 and 2008 in central China. Data were disaggregated by rural and urban hukou. The survival rate of patients was analyzed using Kaplan-Meier method. Prognostic factors were analyzed using the log-rank test and Cox proportional hazards model.


Recruitment information / eligibility

Status Completed
Enrollment 789
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria:

- patients with newly diagnosed prostate cancer were included in the study. Exclusion Criteria:

- Those with a history of prostate cancer who were treated for another disease were excluded from study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China the first affiliated hospital of Zhengzhou University Zhengzhou Henan

Sponsors (13)

Lead Sponsor Collaborator
Zhengzhou University Anyang Regional Hospital, Center hospital of Nanyang, Center hospital of Shangqiu, Center hospital of Zhumadian, First People's Hospital of Kaifeng, Luoyang Central Hospital, People's Hospital of Zhengzhou University, the cancer hospital of Zhengzhou University, The First Affiliated Hospital of Zhengzhou University, Third Affiliated Hospital of Zhengzhou University, Xinyang Central Hospital, Zhoukou Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary overall survival overall survival that was defined as the interval from the date of diagnosis to the Medicare date of death 3 years
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