Effects of INDUS810 on Body Composition, Muscular Performance, and Training Adaptations

Completed · Not applicable · Has a placebo group

Conditions studied: Weakness, Muscle

In brief

The purpose of this 12-week, interventional study is to determine the effects of oral supplementation with Indus810 (dietary supplement with active ingredient Fenugreek) on body composition, muscular performance, and training adaptations

Key facts

Study ID

NCT03850106

Run by

The Center for Applied Health Sciences, LLC

People needed

67

Starts

2018-07-11

Expected to finish

2019-04-30

Last updated by the study team

2020-02-18

Who can join

Age: 18 and older, up to 45. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• Provide voluntary signed and dated informed consent.
• Be in good health as determined by medical history and routine blood chemistries.
• Age between the ages of 18 and 45.
• Body Mass Index (BMI):
• 22-25; Waist:Hip Ratio 0.9-1
• 25-35; Waist:Hip Ratio 0.85-1
• Normotensive (supine, resting systolic blood pressure <140 mm Hg and diastolic blood pressure < 90 mm Hg. If the first measurement is slightly elevated above these limits, the subject will be given a brief (5 minute) rest period, and two more measurements will be taken. The average of all three measurements will be used to determine eligibility.
• Normal supine, resting heart rate (<90 per minute).
• Willing to duplicate their previous 24-hour diet, and fast for 8-10 hours prior each of the treatments.
• Has been participating in regular exercise training, at least 3 days per week, for the past 1-2 months.

You may not qualify if…

• History of diabetes.
• Use of any pre-workout or creatine containing products in the last 4 weeks.
• History of malignancy in the previous 5 years except for non-melanoma skin cancer (basal cell cancer or squamous cell cancer of the skin).
• Prior gastrointestinal bypass surgery (Lapband, etc.).
• Other known gastrointestinal or metabolic diseases that might impact absorption or amino acid metabolism, e.g. short bowel syndrome, diarrheal illnesses, history of colon resection, gastro paresis, Inborn-Errors-of-Metabolism (such as PKU).
• Chronic inflammatory condition or disease (e.g. rheumatoid arthritis, Crohn's disease, ulcerative colitis, Lupus, HIV/AIDS, etc.). -Known sensitivity to any ingredient in the test formulations as listed in the Certificates- of-Analysis.
• Currently participating in another research study with an investigational product or have been in another research study in the past 30 days.
• Concomitant use of corticosteroids or testosterone replacement therapy (ingestion, injection, or transdermal).
• Any other diseases or conditions that, in the opinion of the medical staff, could confound the primary endpoint or place the subject at increased risk of harm if they were to participate.

Where it is running

• The Center for Applied Health Sciences — Stow, Ohio, United States

Full record on ClinicalTrials.gov

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