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Effects of Neo40(TM) With Caffeine on Cycling Time Trial Performance

Effects of Neo40(TM) With Caffeine on Cycling Time Trial Performance

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01710761
Enrollment
16
Registered
2012-10-19
Start date
2012-10-31
Completion date
2013-05-31
Last updated
2013-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

nitric oxide, cycling performance, lactate, VO2

Brief summary

Acute supplementation of Neo40(TM), a nitrate lozenge, will improve cycling performance

Interventions

DIETARY_SUPPLEMENTPlacebo

Same form factor and flavor as test lozenge but contains no active ingredients

DIETARY_SUPPLEMENTNitrate supplement with caffeine

Lozenge consisting of beetroot and 75 mg caffeine

Sponsors

Neogenis Laboratories
CollaboratorOTHER
University of Texas at Austin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Regular commuter cyclist or spin class participant * Male (VO2max \< 50) or Female (VO2max \< 45) * Healthy * Blood pressure below 140/90 * Non-smoker

Exclusion criteria

* Does not cycle 2-3 times/week * Regular consumption of performance-enhancing substances * Type I or Type II diabetes * Renal, hepatic or cardiac disease * Current infectious disease

Design outcomes

Primary

MeasureTime frameDescription
Improved Time Trial PerformanceAfter 20 min steady-state cyclingParticipants will cycle 20 min at increasing intensity: 8 min at 55% VO2max, 6 min at 65% VO2max, 6 min at 75% VO2max. The 20 km time trial consists of rolling hills.

Secondary

MeasureTime frameDescription
Improved work efficiencyDuring 20 min steady-state cyclingExpired gases will be collected and compared to expected VO2. Blood will be collected prior to treatment, prior to exercise and during each cycling intensity to analyze lactate accumulation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026