- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03433092
Serum Carotenoids and Risk of Gastrointestinal Tract Cancer: Meta-analysis of Ten Studies
February 15, 2018 updated by: Yong Zhou
Previous studies have suggested that serum carotenoids may be associated with risk of gastrointestinal tract cancer (GIT cancer), but the results were inconsistent.
Thus, the investigators conducted a meta-analysis to evaluate the associations between serum carotenoids and risk of GIT cancer.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
40641
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sichuan
-
Chengdu, Sichuan, China, 610041
- West China Hospital, Sichuan University
-
-
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
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The study population include people from primary care clinic or community sample.
Description
Inclusion Criteria:
- The study had both case and control groups
- Serum carotenoids levels, relative risk (RR) or OR and corresponding 95% CI were reported
- Patients in case group were diagnosed with GIT cancer
Exclusion Criteria:
·Animal studies
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Jing Huang et. al, 2017
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
Max Leenders et. al,2014
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
Yusuke Okuyama et. al,2014
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
GC Kabat et. al,2012
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
Christina Persson et. al,2008
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
M Jenab et. al,2006
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
Kenji Wakai et. al,2005
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
Christian C. Abnet et. al,2003
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
N Malila et. al,2002
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
|
G Pappalardo et. al,1997
|
In each study, the serum concentrations of carotenoids were detected by high performance liquid chromatography
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gastrointestinal Tract Cancer Incident Measure
Time Frame: Through study completion, an average of 5 years.
|
The gastrointestinal tract cancer incident would be recorded during the follow-up years.
|
Through study completion, an average of 5 years.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)
November 1, 2017
Primary Completion (Actual)
November 20, 2017
Study Completion (Actual)
December 28, 2017
Study Registration Dates
First Submitted
February 7, 2018
First Submitted That Met QC Criteria
February 7, 2018
First Posted (Actual)
February 14, 2018
Study Record Updates
Last Update Posted (Actual)
February 22, 2018
Last Update Submitted That Met QC Criteria
February 15, 2018
Last Verified
February 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2759067085
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.