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OpenTrials
Completed

NCT Number: NCT00749983

Effects of Creatine Supplementation in Women With Knee Osteoarthritis and Fibromyalgia

The purpose of this study is to determine whether creatine associated or not to exercise training can improve physical performance in patients with knee osteoarthritis and fibromyalgia.

Completed

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Key information

Age range

25 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Sao Paulo School of Medicine

São Paulo, 01246903, Brazil

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fulfill ACR criteria of knee osteoarthritis
  • Fulfill ACR criteria of fibromyalgia

Exclusion criteria

  • Athletes
  • Drugs stable for at least three months before entering the study
  • No limitations to resistance training

Treatment and study plan

creatine supplementation

Dietary Supplement

Dextrose supplementation

Dietary Supplement

Primary outcomes

  1. Physical function

    Time frame: 12 weeks

    Assessed by the timed-stands test

Secondary outcomes

  1. Strength

    Time frame: 12 weeks

    Assessed by the 1-repetition maximum test

  2. Quality of life

    Time frame: 12 weeks

    health-related questionaires

  3. Body composition

    Time frame: 12 weeks

    Assessed by DXA

  4. Renal function

    Time frame: 12 weeks

    Assessed by 51Cr-EDTA

Sponsors and collaborators

Lead sponsor

University of Sao Paulo

Other

Registry information

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Sep 10, 2008
Registry last updated
Oct 2, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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