Guanidinoacetic Acid (GAA) Administration in Physically Active Men and Women
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ClinicalTrials.gov Identifier: NCT01133899 |
Recruitment Status :
Completed
First Posted : May 31, 2010
Last Update Posted : December 20, 2011
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Athletic Performance | Dietary Supplement: guanidinoacetic acid Dietary Supplement: GAA-4 Dietary Supplement: GAA-1 Dietary Supplement: PLACEBO | Phase 1 Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 40 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Basic Science |
Official Title: | The Effects of Medium-term Oral Guanidinoacetic Acid (GAA) Administration on Human Performance, Body Composition, and Metabolic Outcomes in Physically Active Men and Women |
Study Start Date : | March 2010 |
Actual Primary Completion Date : | December 2011 |
Actual Study Completion Date : | December 2011 |
Arm | Intervention/treatment |
---|---|
Experimental: GAA-2
2.4 grams of guanidinoacetic acid
|
Dietary Supplement: guanidinoacetic acid
2.4 grams of guanidinoacetic acid |
Experimental: GAA-1
1.2 grams of guanidinoacetic acid
|
Dietary Supplement: GAA-1
1.2 grams of guanidinoacetic acid |
Experimental: GAA-4
4.8 grams of guanidinoacetic acid
|
Dietary Supplement: GAA-4
4.8 grams of guanidinoacetic acid |
Placebo Comparator: PLACEBO
cellulose
|
Dietary Supplement: PLACEBO
celulose |
- Muscle power [ Time Frame: Baseline, at 1 week, at 2 weeks, at 4 weeks, at 6 weeks, at 8 weeks, at 10 weeks ]The majority of investigations involving the effects of creatine (or creatine precursors) supplementation on human performance were laboratory-based and have focused on musucular strength and power and anaerobic endurance, with various task protocols such as weght lifting, running, jumping and cycling less than or equal to 30 sec in duration. Similarly, the effects of GAA on exercise performance should be investigated with measuring muscle strength and power (through both isometric and isotonic exercise) and anaerobic endurance (e.g. repeated jumping performance).
- Muscle mass [ Time Frame: Baseline, at 1 week, at 2 weeks, at 4 weeks, at 6 weeks, at 8 weeks and at 10 weeks ]A creatine supplementation-induced increase in body mass, particularly if not muscle mass, could be detrimental to performance in sports in which the body mass needs to be moved efficiently from one point to another. If GAA acts as creatine, which is an osmotically active substance, an increase in intracellular creatine concentration may likely induce influx of water into the cell. Therefore, changes of body mass and body composition (particularly muscle mass) after GAA intake should be monitored during the present study.

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Ages Eligible for Study: | 20 Years to 25 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- healthy young men and women
- aged 20 to 25 years
- experienced in athletic training
- free from musculoskeletal dysfunctions
- free from metabolic and heart diseases
- participating in consistent training (average of three times per week)
Exclusion Criteria:
- current intake of dietary supplement containing performance-enhancing agent
- pregnant women
- current intake of hormonal contraceptives

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01133899
Serbia | |
Biomedical Scinces Department, Exercise Physiology Lab | |
Novi Sad, Vojvodina, Serbia, 21000 |
Principal Investigator: | Sergej M Ostojic, MD, PhD | Biomedical Sciences Dept, Faculty of Sport Sciences and Tourism, Metropolitan University |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Sergej M. OSTOJIC, Heaf of Exercise Physiology Lab, Metropolitan University, Serbia |
ClinicalTrials.gov Identifier: | NCT01133899 |
Other Study ID Numbers: |
AN-85E-S09 |
First Posted: | May 31, 2010 Key Record Dates |
Last Update Posted: | December 20, 2011 |
Last Verified: | December 2011 |
strength, anaerobic performance, recovery, ergogenic |