The Association of G9a Protein and the Outcome of Patients With Cervical Cancer
1 other identifier
observational
69
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2012
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 27, 2011
CompletedFirst Posted
Study publicly available on registry
January 9, 2012
CompletedStudy Start
First participant enrolled
February 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2015
CompletedSeptember 7, 2016
July 1, 2015
3 years
December 27, 2011
September 4, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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
Secondary Outcomes (1)
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
Study Arms (1)
cervical cancer
Eligibility Criteria
Patients with cervical cancer, and underwent primary treatment (surgery, radiotherapy or chemotherapy) in Far Eastern Memorial Hospital
You may qualify if:
- cases with cervical cancer
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital
Banqiao District, New Taipei, 22050, Taiwan
Biospecimen
Residual pathology block after pathological exam
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief, Department of Obstetrics & Gynecology
Study Record Dates
First Submitted
December 27, 2011
First Posted
January 9, 2012
Study Start
February 1, 2012
Primary Completion
February 1, 2015
Study Completion
February 1, 2015
Last Updated
September 7, 2016
Record last verified: 2015-07