- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03447028
Effect of TyG Index on Outcomes of Radical Prostatectomy (TyG-PCa)
February 24, 2018 updated by: Mustafa Ozan HORSANALI, Recep Tayyip Erdogan University Training and Research Hospital
A Novel Prognostic Risk Factor for Patients Undergoing Radical Prostatectomy: Triglyseride-Glucose (TyG) Index
We investigate the association between Triglyserid-Glucose(TyG) index and prostate cancer in patients undergoing radical prostatectomy.
Study Overview
Status
Completed
Conditions
Detailed Description
TyG index is calculated with special formula.
Patients undergoing radical prostatectomy are divided two groups according to the cut-off level of 8.55 for TyG index.Groups were compared statistically in terms of oncological outcomes and survival.
Study Type
Observational
Enrollment (Actual)
200
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
patients undergoing radical prostatectomy for prostate cancer between january 2007 and december 2012.
Description
Inclusion Criteria:
- Patients undergoing radical prostatectomy for prostate cancer
Exclusion Criteria:
- taking medicines for established diabetes and dyslipidaemia,
- presence of endocrinological disease,
- history of bariatric surgery,
- missing data and patients with uncontrolled follow-up
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Oncological outcomes
Time Frame: 5 years
|
Effect of TyG index on oncological outcomes of Prostate cancer
|
5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Survival
Time Frame: 5 years
|
Death date of patient after radical prostatectomy
|
5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2007
Primary Completion (Actual)
December 30, 2012
Study Completion (Actual)
December 30, 2012
Study Registration Dates
First Submitted
February 20, 2018
First Submitted That Met QC Criteria
February 24, 2018
First Posted (Actual)
February 27, 2018
Study Record Updates
Last Update Posted (Actual)
February 27, 2018
Last Update Submitted That Met QC Criteria
February 24, 2018
Last Verified
February 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Recepteutrh
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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