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Plasma Amino Acid Response to Whey Protein Ingestion Following 28-days of Probiotic Supplementation

L

Lipscomb University

Status

Completed

Conditions

Focus of Study is Amino Acid Appearace in Blood

Treatments

Dietary Supplement: Placebo
Dietary Supplement: Bacillus subtilis DE111

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT04491188
01082018

Details and patient eligibility

About

Active males and females consumed a probiotic for 28-days. Before and after the intervention period, participants reported to the lab in a fasted state where they consumed 25 grams of whey protein. Following drink consumption, participants provided blood draws at 15-minute intervals. Blood samples were analyzed for amino acid concentrations.

Enrollment

22 patients

Sex

All

Ages

18 to 34 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-34 years old Participants must have at least 1 year of resistance training experience.
  • Free of any physical limitations, medications, and supplements that may affect performance, as determined by a health and activity questionnaire.
  • Are free of musculoskeletal injuries
  • Are not taking medications that may interfere with study measurements

Exclusion criteria

  • Taking any other nutritional supplement or performance enhancing drug.
  • Any chronic illness that causes continuous medical care
  • Taking any other nutritional supplement or performance enhancing drug.
  • Any chronic illness that causes continuous medical care.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

22 participants in 2 patient groups, including a placebo group

Probiotic
Experimental group
Description:
1 x10-9 CFU Bacillus subtilis DE111 was consumed daily for 28-days
Treatment:
Dietary Supplement: Bacillus subtilis DE111
Placebo
Placebo Comparator group
Description:
Maltodextrin placebo was consumed for 28-days
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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