Lindenwood University
Lindenwood University sponsors 29 registered US clinical trials on ClinicalTrials.gov, 4 of them currently recruiting, and 22 completed. The most-studied condition in this pipeline is Hypertrophy, with 2 trials.
Trial Pipeline
29 total, page 1 of 1
A Pilot Study to Evaluate the Ability of Lactoferrin to Modulate Iron Homeostasis and Exercise Performance in Exercising Females
NCT07546591
Impact of Weizmannia (Bacillus) Coagulans JBI-YZ6.3 on Gut Health and Fecal Microbiome Changes
NCT07388264
Dose-Response Impact of Glucosyl-Hesperidin (CitraPeak) on Exercise Performance, Blood Flow, Stress, Cognition, and Other Perceptual Indicators
NCT06672952
Dose-Response Impact of Geranylgeraniol (GG) Supplementation on Muscle Health
NCT07502924
Evaluating the Ability of a Multi-Strain Postbiotic to Impact Inflammation, Immune Components, Gastrointestinal Symptoms, Recovery, Anxiety, and Intestinal Permeability
NCT07387991
Evaluation of Cordyceps Militaris M2-116-04 for Its Potential Sport and Exercise Nutrition Applications in Healthy Active Adults
NCT07310108
A Randomized, Double-Blind Study to Assess the Effect of a Postbiotic on Oxidative Stress and Exercise Performance
NCT06795425
Exercise-Induced Rates of Fat Oxidation with and Without Ingestion of a Caffeine-Based Energy Drink
NCT06308731
Effects of Alpha-GPC on Muscle Power, GH Levels, and Cognitive Function
NCT06690619
A Randomized Study to Examine the Ability of a Caffeine-Based Energy Drink to Impact Energy Expenditure, Fat Oxidation, Reaction Time, and Other Perceptual Indicators
NCT05998096
Impact of Powdered Tart Cherries on Recovery From Repeated Sprints
NCT06122038
Effects of Adding L-BAIBA or L-BAIBA + Grains of Paradise to Exercising Adult Overweight and Obese Men and Women
NCT05775003
Effects of Adding L-BAIBA to Exercising Adult Overweight and Obese Men and Women
NCT05775016
Kefir Versus Milk on Time-Trial Performance in Masters Athletes
NCT06165523
Effect of a Novel Blend of Plant Protein and Additional Ingredients on Resistance Training Adaptations
NCT06908811
A Prospective, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of LasoperinTM on Cognitive Function in Healthy Adults
NCT05994391
Pilot Study to Examine the Acute Impact of Veillonella Supplementation on Exercise and Lactate Responses
NCT05816291
Changes in Metabolic Rate and Perceptual Indicators After Acute Ingestion of Paraxanthine
NCT05811923
Dose-Response Effect of Phosphatidylserine on eSport Performance
NCT07533032
Effects of Paraxanthine Supplementation on eSport Performancre
NCT07533045
Dileucine and Resistance Training Adaptations
NCT06121869
Changes in Plasma Amino Acid Appearance After Adding Bacillus Coagulans GBI-30, 6086 to Milk Protein Concentrate
NCT05313178
A Pilot Study to Determine the Bioavailability of Oral Beta-Aminoisobutyric Acid (BAIBA) Ingestion
NCT05328271
Effect of the Combination of Nitrate and Caffeine on Critical Power In Trained Male Cyclists
NCT07501806
Bioavailability of Berberine and Dihydroberberine and Their Impact on Glycemia
NCT05021341
Changes in Amino Acid Absorption After Adding a Probiotic to an Acute Protein Feeding
NCT04427020
Probiotic Administration on Mood
NCT05343533
Immune and Recovery Modulating Impact of Probiotic Supplementation After Intense Resistance Exercise
NCT04441840
Effect of Daily Doses of Rice or Whey Protein on Resistance Training Adaptations
NCT04411173
Therapeutic Areas
What the Pipeline for Lindenwood University Shows
According to the ClinicalTrials.gov registry, Lindenwood University is linked to 29 US clinical trials across every stage of research activity. Of those, 4 studies are currently recruiting, about 14% of the sponsor's indexed portfolio, and 22 are already marked complete, representing roughly 76% of the total.
The phase mix for Lindenwood University reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Lindenwood University is Hypertrophy with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.