The Effects of VEGF-B Signaling Pathway in Obesity and Metabolic Disease
Obesity
1 other identifier
observational
194
1 country
1
Brief Summary
The investigators will enroll about 120 subjects from the hospital's healthcare center. The investigators will collect the basic informations, blood pressure, body mass index, fasting blood glucose and fasting blood lipids of each subject. The investigators will collect the blood samples and then test them for fasting insulin levels, VEGF-B levels, the gene promoter region methylation status and the genomic protein methylation levels of the VEGF-B gene of the cells,and finally do the statistical analysis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2017
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 20, 2017
CompletedFirst Submitted
Initial submission to the registry
May 13, 2017
CompletedFirst Posted
Study publicly available on registry
May 23, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2018
CompletedApril 8, 2021
April 1, 2021
4 months
May 13, 2017
April 5, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Fasting insulin and blood VEGF-B levels
To investigate the relationship between blood pressure, BMI, fasting blood glucose, fasting blood lipids and fasting insulin and blood VEGF-B levels.
3 days
Secondary Outcomes (1)
The methylation status of VEGF-B gene promoter region and VEGF-B genomic protein methylation level .
7 days
Study Arms (2)
Group 1
subjects without metabolic diseases
Group 2
subjects with metabolic diseases
Eligibility Criteria
subjects without metabolic diseases , subjects with metabolic diseases
You may not qualify if:
- subjects with active history insulin treatment; and female participant pregnant at the time of recruitment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Endocrinology, Union Hospital,Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China
Biospecimen
Plasma,Peripheral blood mononuclear cells
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chen Lulu
Department of Endocrinology, Union Hospital,Tongji Medical College, Huazhong University of Science and Technology
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of Endocrinology
Study Record Dates
First Submitted
May 13, 2017
First Posted
May 23, 2017
Study Start
April 20, 2017
Primary Completion
September 1, 2017
Study Completion
March 1, 2018
Last Updated
April 8, 2021
Record last verified: 2021-04
Data Sharing
- IPD Sharing
- Will not share