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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02325271
Other study ID # VEGF Bio
Secondary ID
Status Completed
Phase N/A
First received December 19, 2014
Last updated September 4, 2017
Start date February 2015
Est. completion date January 2016

Study information

Verified date September 2017
Source GWT-TUD GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study evaluates the intra-individual variability of VEGF levels over a period of 6 months as well as the circadian variation of VEGF levels, both under standardized conditions in patients with type 2 diabetes without DME and matched subjects with normal glucose tolerance (NGT). Secondary objectives of the study are to evaluate the relationship of individual VEGF-levels to biomarkers of inflammation, HbA1c and major cardiovascular risk factors.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 2016
Est. primary completion date October 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

- Written informed consent

- Age equal to or between 50 and 80 years

- Subjects with normal glucose tolerance confirmed by glucose tolerance test (control group) or patients with type 2 diabetes: diabetes duration 5-25 years; HbA1c equal to or between 6.5 and 9% (diabetes group)

- Ability to understand and follow study-related instructions

Exclusion Criteria:

- DME

- hsCRP > 10 mg/dl

- Acute infections

- Acute or chronic inflammatory diseases

- Immune diseases

- Treatment with immune suppressive drugs

- Treatment with glucocorticoids

- Myocardial infarction and stroke within 1 year before inclusion

- Hemorrhage within the previous 5 years

- Surgeries within the previous 3 months

- Oncological diseases

- Women who are pregnant or breast-feeding

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Frequent blood and urine sampling and blood pressure measurement
Blood and urine sampling for the determination of VEGF and biomarkers

Locations

Country Name City State
Germany GWT-TUD GmbH / Studienzentrum Hanefeld Dresden

Sponsors (2)

Lead Sponsor Collaborator
GWT-TUD GmbH Novartis

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary VEGF-A Plasma levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Primary VEGF-B Plasma levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Primary VEGF-C Plasma levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Primary Placental growth factor Plasma levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Primary VEGF-A Plasma levels determined over the day Hourly over 12 hours
Primary VEGF-B Plasma levels determined over the day Hourly over 12 hours
Primary VEGF-C Plasma levels determined over the day Hourly over 12 hours
Primary Placental growth factor Plasma levels determined over the day Hourly over 12 hours
Secondary Glycated hemoglobin (HbA1c) Plasma levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Secondary High-sensitivity C-reactive protein (hCRP) Serum levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Secondary Matrix metallopeptidase 9 (MMP-9) Plasma levels determined in the morning under fasted conditions Baseline, month 1, 2, 3, 4, 5 and 6
Secondary MMP-9 Plasma levels determined over the day Hourly over 12 hours
Secondary Adiponectin Serum levels determined in the morning under fasted condition Baseline, month 1, 2, 3, 4, 5 and 6
Secondary Adiponectin Serum levels determined over the day Hourly over 12 hours
Secondary Cystatin C Serum levels determined in the morning under fasted condition Baseline, month 1, 2, 3, 4, 5 and 6
Secondary Cystatin C Serum levels determined over the day Hourly over 12 hours
Secondary Albumin Urine levels determined in the morning under fasted condition Baseline, month 1, 2, 3, 4, 5 and 6
Secondary Creatinine Urine levels determined in the morning under fasted condition Baseline, month 1, 2, 3, 4, 5 and 6
Secondary Creatinine Serum levels determined in the morning under fasted condition Baseline, month 1, 2, 3, 4, 5 and 6
Secondary Blood pressure Baseline, month 1, 2, 3, 4, 5 and 6, once over 24 hours
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