- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01113827
Effects of Water-soluble Olive Extract Supplementation
March 23, 2012 updated by: University of Texas at Austin
Effects of Water-soluble Olive Extract on Antioxidant Status, Exercise Performance, Muscle Metabolism, Muscle Damage and Inflammation
Six weeks of supplementation of an olive extract will:
- Improve antioxidant status
- Reduce inflammation
- Reduce muscle damage
- Improve exercise performance
- Improve exercise recovery as compared to a placebo.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
61
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Texas
-
Austin, Texas, United States, 78712
- The University of Texas at Austin
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 35 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Recreational exerciser
- BMI <= 30
- Non-smoker
Exclusion Criteria:
- Blood pressure over 140/90
- Type I or Type II diabetes
- Renal, hepatic or cardiac disease
- Current infectious disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Placebo control
|
Placebo
|
|
Active Comparator: 150mg olive extract
|
Capsule form ingested 1x/day for 6 weeks
|
|
Active Comparator: 50mg olive extract
|
Capsule form ingested 1x/day for 6 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Improved Antioxidant Status
Time Frame: 6 weeks
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Reduced Inflammation
Time Frame: 6 weeks
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: John Ivy, Ph.D., The University of Texas at Austin
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2010
Primary Completion (Actual)
July 1, 2011
Study Completion (Actual)
February 1, 2012
Study Registration Dates
First Submitted
April 28, 2010
First Submitted That Met QC Criteria
April 29, 2010
First Posted (Estimate)
April 30, 2010
Study Record Updates
Last Update Posted (Estimate)
March 27, 2012
Last Update Submitted That Met QC Criteria
March 23, 2012
Last Verified
February 1, 2012
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2009-09-01-OLIV
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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