Title

The Effect of XSurge Supplementation on Biomarkers and Performance From High Intensity Resistance Exercise
The Effect of XSurgeTM Supplementation on Biomarkers, Oxidative Stress, and Recovery From High Intensity Resistance Exercise
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    cellulose ...
  • Study Participants

    41
Part one of this study will consist of baseline (BL) testing, 28 days of daily supplementation with XSurge, and an exercise protocol. The acute exercise protocol consists of five visits, of which, the first visit will consist of maximal strength testing. The remaining visits will consist of performance testing and muscle evaluation.

Phase two of this study will consist of six weeks of supervised resistance training along with supplementation of XSurge. Following the six weeks of training, subjects will complete a second acute exercise protocol. Measures to be evaluated will consist of performance testing and muscle evaluation.
Study Started
Feb 28
2015
Primary Completion
Feb 29
2016
Study Completion
Aug 31
2016
Last Update
Jan 31
2018

Dietary Supplement XSurge

During part one of the study, 28 days of supplementation with XSurge will be provided. During the second part of the study 6 weeks of supplementation with XSurge will accompany a training program.

Other Placebo: Microcrystalline Cellulose

Other Control: No supplementation

Placebo Placebo Comparator

Placebo group will receive microcrystalline cellulose

Treatment Active Comparator

Treatment group will get 2 g daily of XSurge in microcrystalline cellulose

Control Group Sham Comparator

The control group will be included to quantify or describe the effects of the acute exercise training but will not receive any supplement

Criteria

Inclusion Criteria:

Recreationally active.
Subject is judged by the Investigator to be healthy and free of any physical limitations
Subject is male 18-35 y of age, inclusive
Subject has a body mass index of 18.0-34.9 kg/m2
Subject is willing to maintain habitual diet
Subject is willing to abstain from dietary supplementation
Subject understands the study procedures and signs forms providing informed consent to participate in the study and authorization for release of relevant protected health information to the study Investigators

Exclusion Criteria:

Subject is currently or will be enrolled in another clinical trial.
Subject has a history or presence of a clinically relevant cardiac, renal, hepatic, endocrine (including diabetes mellitus), pulmonary, biliary, gastrointestinal, pancreatic, or neurologic disorder.
Subject has a history or presence of cancer in the prior 2 years, except for non-melanoma skin cancer.
Subject is unable to perform physical exercise
Subject is a current smoker or has quit within the last 6 months
Subject is engaged in an extreme diet including but not limited to, Atkins, South Beach, Intermittent Fasting, etc.
Subject is allergic to the study product or placebo
Subject is taking any other nutritional supplement or performance enhancing drug
Subjects that have donated blood or plasma within the previous week
Subject has any chronic illness that causes continuous medical care
Taking any type of prescription or over-the-counter medication including but not limited to corticosteroids, non-steroidal anti-inflammatory drugs, and antibiotics within the 14 days prior to the screening visit.
No Results Posted