- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02627898
Effect of Green Tea Extract on Arterial Stiffness in Type 2 Diabetes Mellitus
January 23, 2018 updated by: Fernando Grover Paez, Centro Universitario de Ciencias de la Salud, Mexico
Effect of Green Tea Extract Administration on Arterial Stiffness in Patients With Type 2 Diabetes Mellitus
Type 2 diabetes mellitus (T2DM) has become the epidemic of the XXI century.
This chronic disease is also highly prevalent and primarily associated with an increased cardiovascular mortality and morbidity due to micro and macrovascular complications, where its pathophysiological mechanism accelerates the formation of the atherosclerotic process, fundamental element associated with arterial stiffness.
The importance of anticipating the presence of a cardiovascular event lies precisely in the early detection of subclinical changes in the elastic arteries identified by measuring the pulse wave velocity.
Having adequate pharmacological or non-pharmacological interventions that impact precisely in the reduction of pulse wave velocity contributes to a reduction of cardiovascular morbidity and mortality associated with DM2.
Among non-pharmacological therapies they have been studied the benefits attributed to the use of green tea infusion either encapsulated or extract have been associated mainly with anti-inflammatory and antioxidant effects.
There are both experimental and clinical studies that have shown benefits of administration of green tea (extract or infusion), and administered by different routes at different dosages and for varying times.
But it has been noted that not all studies with green tea meet appropriate to draw conclusions about its benefits to cardiovascular level.
However, it is proposed that the use of green tea extract with a highest amount of catechins through a controlled clinical trial could be a potential therapeutic strategy for changing hemodynamic alterations and arterial stiffness favorably in this particular group of patients DM2.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The objetive is to evaluate the effect of administration of Green tea exctract on arterial stiffness in individuals with T2DM.
The investigators will conduct a double-blind trial, randomized, placebo control group, each group 12 male and female patients of 35-65 years of age with T2DM, with no hypertension or treated with insulins.
Randomization will determine who will receive the intervention during 8 week trial (Green tea extract capsule, 400 mg 1 time daily with the first bite of each meal or approved placebo capsules), both groups also will continue with their usual treatment.
The clinical findings and laboratory test include a metabolic profile and biosafety, wich will be baseline and at 8 weeks.
Body weight, body fat, body mass index (BMI) and blood pressure will be determined during the inicial and final visit, likewise, hemodynamics parameters of arterial stiffness like the aortic pulse wave velocity (PWVao), central pulse pressure (PPao), aortic augmentation index (IAxao) and central systolic blood pressure (cSBP) by an oscillometric monitoring system via BPLab ®.
Adverse events and adherence to treatment will be documented.
The statistical analysis: Mann-Whitney U Test and Wilcoxon exact test.
It is considered with significance at p<0.05.
Study Type
Interventional
Enrollment (Actual)
24
Phase
- Phase 2
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
35 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Diagnosis of T2DM
- Fasting plasma glucose >126 and <250 mg/dl at the time security
- Metformin monotherapy or with glibenclamide added
- Written informed consent
Exclusion Criteria:
- Hypertention
- Treated with insulin
- Use of antioxidant suplements or products with caffeine
- Woman pregnant or breastfeeding
- Untreated tyroid disease
- Total colesterol >400mg/dl
- Triglycerides >400mg/dl
- Liver enzimes (alt and ast) more tan twice the normal range
- Glomerular filtration rate <60ml/min (Cockcroft-Gault)
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
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Green tea extract
Individuals with T2DM controlled with metformin or glibenclamide, or both; with no hypertension neither treated with insulim
|
Green tea extract capsules, 400mg 1 time daily with the first bite of eat meal
Other Names:
|
|
PLACEBO_COMPARATOR: Placebo
Individuals with T2DM controlled with metformin or glibenclamide, or both; with no hypertension neither treated with insulim
|
Placebo capsules, 400mg 1 time daily with the first bite of eat meal
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Aortic Pulse Wave Velocity measured in meters / second, at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention with oscillometric monitoring system via BPLab
|
baseline and 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in aortic pulse pressure measured in mm / Hg at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention with oscillometric monitoring system via BPLab
|
baseline and 12 weeks
|
|
Change from Baseline in aortic Augmentation index measured in percentage at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention with oscillometric monitoring system via BPLab
|
baseline and 12 weeks
|
|
Change from Baseline in central systolic blood pressure measured in mm / Hg at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention with oscillometric monitoring system via BPLab
|
baseline and 12 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Fasting plasma glucose measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by spectrophotometry
|
baseline and 12 weeks
|
|
Change from Baseline in Total cholesterol measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by spectrophotometry
|
baseline and 12 weeks
|
|
Change from Baseline in Triglycerids measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by spectrophotometry
|
baseline and 12 weeks
|
|
Change from Baseline in High-density lipoprotein colesterol measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by friedewall formula
|
baseline and 12 weeks
|
|
Change from Baseline in Low-density lipoprotein colesterol measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by friedewall formula
|
baseline and 12 weeks
|
|
Change from Baseline in Alanine aminotransferase measured in IU / L at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by spectrophotometry
|
baseline and 12 weeks
|
|
Change from Baseline in Aspartate aminotransferase measured in IU / L at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by spectrophotometry
|
baseline and 12 weeks
|
|
Change from Baseline in Creatinine measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention by spectrophotometry
|
baseline and 12 weeks
|
|
Change from Baseline in Peripheral systolic blood pressure measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention using a digital baumanometer
|
baseline and 12 weeks
|
|
Change from Baseline in Peripheral diastolic blood pressure measured in mg / dL at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention using a digital baumanometer
|
baseline and 12 weeks
|
|
Change from Baseline in Body and visceral fat measured in centimeters ^ 2 at 12 weeks
Time Frame: baseline and 12 weeks
|
Before and after intervention using an impedance bascula, Dualscan HDS-2000
|
baseline and 12 weeks
|
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
January 1, 2016
Primary Completion (ACTUAL)
September 1, 2016
Study Completion (ACTUAL)
December 1, 2016
Study Registration Dates
First Submitted
December 3, 2015
First Submitted That Met QC Criteria
December 10, 2015
First Posted (ESTIMATE)
December 11, 2015
Study Record Updates
Last Update Posted (ACTUAL)
January 25, 2018
Last Update Submitted That Met QC Criteria
January 23, 2018
Last Verified
January 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CUCS-INTEC-MV-TEVE-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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