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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04144114
Other study ID # Pro18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date December 7, 2018

Study information

Verified date October 2019
Source Deerland Enzymes
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To examine the amino acid absorption following acute resistance exercise between three supplemental treatments: 1) Whey Protein + ProHydrolase (WPH) 2) Whey Protein (W) and 3) Non-Caloric Placebo (PL). To examine three supplemental treatments (WPH, W, PL) in conjunction with acute resistance exercise on the mTORC1 complex pathway. To examine three supplemental treatments (WPH, W, PL) in conjunction with acute resistance exercise on circulating concentrations of endocrine biomarkers.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date December 7, 2018
Est. primary completion date December 7, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- • At least one-year of resistance training experience

- Free of any physical limitations (determined by health and activity questionnaire).

- Between the ages of 18 and 35.

- Ability to leg press a weight equivalent to 1.5 times their body mass

Exclusion Criteria:

- • Inability to perform physical exercise (determined by health and activity questionnaire)

- Taking any other nutritional supplement or performance enhancing drug (determined from health and activity questionnaire).

- Physical injury preventing the athlete from participating in offseason training

- Any chronic illness that causes continuous medical care

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
ProHydrolase®
Subjects received 250mg of ProHydrolase® with 25g whey protein mixed together in a drink
Whey protein
Subjects received 25g of whey protein powder mixed to together in a drink
Placebo
Placebo

Locations

Country Name City State
United States Lipscomb University Nashville Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Deerland Enzymes Lipscomb University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amino acid absorption To examine the amino acid absorption following acute resistance exercise between three supplemental treatments: 1) Whey Protein + ProHydrolase (WPH) 2) Whey Protein (W) and 3) Non-Caloric Placebo (PL) 4 weeks
Primary mTORC1 pathway To examine three supplemental treatments (WPH, W, PL) in conjunction with acute resistance exercise on the mTORC1 complex pathway 4 weeks
Primary Endocrine markers To examine three supplemental treatments (WPH, W, PL) in conjunction with acute resistance exercise on circulating concentrations of endocrine biomarkers. 4 weeks
See also
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