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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01505751
Other study ID # 100078-E
Secondary ID
Status Completed
Phase N/A
First received December 27, 2011
Last updated September 4, 2016
Start date February 2012
Est. completion date February 2015

Study information

Verified date July 2015
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

G9a protein was approved to be highly associated with recurrence of breast cancer, gastric cancer, hepatocellular cancer, prostate cancer and lung cancer. Therefore, the aim of this study was to clarify the association and G9a protein and cervical cancer by analyzing the immunohistochemical staining of G9a protein to the histopathologic specimen of cervical cancer and clinical data.


Recruitment information / eligibility

Status Completed
Enrollment 69
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 99 Years
Eligibility Inclusion Criteria:

- cases with cervical cancer

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary determine whether G9a protein is a risk factor of overall survival of patients with cervical cancer From the date of primary treatment until the date of death from any cause or the date of last follow-up, whichever came first, assessed up to 100 months No
Secondary determine whether G9a protein is a risk factor of progression-free survival of patients with cervical cancer From the date of primary treatment until the date of first documented progression or last follow-up, whichever came first, assessed up to 100 months No
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