Effect of Cassia Cinnamon on Arterial Stiffness Parameters in Patients With Type 2 Diabetes Mellitus
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- STATUS
- Recruiting
-
- participants needed
- 30
-
- sponsor
- University of Guadalajara
Summary
Many nutraceuticals have been currently implemented aimed to improve glycemic control, and
reduce cardiovascular risk and its complications, which results in a better quality of life
in patients with
Cassia cinnamon pulverized bark has demonstrated to have
Description
A randomized, placebo control group, double blind clinical trial. 30 patients (male or
female) from 40 to 65 years old with
All patients should give written informed consent prior to be enrolled. The protocol was previously approved by the local ethics committee (Experimental and Clinical Therapeutic Institute) of University of Guadalajara, registration number: CEI/489/2019. Patients with other medical conditions, taking additional drugs or with more than 1 year of evolution will be excluded.
- Procedure
The entire study consists of a total of 5 visits, the first one (day - 7) is the screening visit where written informed consent, clinical history, anthropometric measurements and blood samples will be performed.
The second or initial visit (day 0) consists of review of laboratory results, hemodynamic
studies (i.e brachial - ankle pulse wave velocity and index for
The third and fourth visits (day 30 and 60) consist of evaluation of treatment adherence,
side effects,
The fifth and last visit (day 90) is similar to day 0 plus evaluation of treatment adherence and side effects. This is the end of intervention period.
Details
| Condition |
|
|---|---|
| Age | 40years - 65years |
| Treatment | Cassia Cinnamon, Calcined magnesia |
| Clinical Study Identifier | NCT04259606 |
| Sponsor | University of Guadalajara |
| Last Modified on | 19 February 2024 |
How to participate?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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