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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00992043
Other study ID # eefeusp2
Secondary ID
Status Completed
Phase N/A
First received October 7, 2009
Last updated March 22, 2010
Start date October 2009
Est. completion date January 2010

Study information

Verified date October 2009
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Creatine supplementation is capable of improving glucose tolerance in healthy subjects. The researchers aim to investigate whether this supplement can affect metabolic control in diabetic patients.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date January 2010
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 45 Years and older
Eligibility Inclusion Criteria:

- males and females type 2 diabetic patients

- glycated hemoglobin between > 9%

- non insulin users

- physically inactive

- only metformin and/or sulfonylurea users

- BMI > 30 kg/m2

- age of years > 50 y

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
creatine

Other:
Exercise training


Locations

Country Name City State
Brazil General Hospital - School of Medicine - University of Sao Paulo Sao Paulo

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary glycated hemoglobin three months No
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