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Clinical Trials/NCT00992043
NCT00992043CompletedNot Applicable

Efficacy and Safety of Creatine Supplementation Combined With Exercise Training in Type 2 Diabetic Patients

University of Sao Paulo1 site in 1 country28 target enrollmentStarted: October 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
28
Locations
1
Primary Endpoint
glycated hemoglobin

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
45 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Exclusion Criteria

  • Not provided

Arms & Interventions

exercise and placebo

Placebo Comparator

Intervention: Exercise training (Other)

exercise and creatine

Experimental

Intervention: Exercise training (Other)

exercise and placebo

Placebo Comparator

Intervention: creatine (Dietary Supplement)

exercise and creatine

Experimental

Intervention: creatine (Dietary Supplement)

Outcomes

Primary Outcomes

glycated hemoglobin

Time Frame: three months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (1)

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