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CompletedNCT06531070Updated Mar 27, 2025

Nitrate Formulations and Exercise Performance

An interventional study of Nitrate in Nitrate, Nitrate/Citrulline and Placebo, sponsored by University of Greenwich. Completed at 1 site in United Kingdom. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-27.

Sponsored by University of Greenwich · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

this study compares the acute effects of Nitrate and Nitrate plus citrulline supplementation on physical performance in recreationally trained males and females. This is a cross-over within-participant comparison design concluding three arms (i) 600 mg of Nitrate (N), ii) 600 mg Nitrate and Citrulline (NC) and (iii) Placebo (PL).

Conditions N, NC and PL will be tested one week apart, considering a minimum washout period of 72 hours.

Dependent variables:

  • Number of completed repetitions to failure in squat using 75% of 1RM.
  • Ventilatory thresholds (VT1) and (VT2) and Vo2 max from a progressive to exhaustion running test (PGT)
  • Lactate post (within 1 min of having completed the PGT)
  • Rating of perceived exertion (RPE) by the Borg 6-to-20-point scale recorded every 2 min and at the end of the PGT.
  • Heart rate associated with VT1, VT2, and Vo2max - Heart rate maximum.
  • Maximal aerobic speed (MAS): calculated from the average speed of the last 2 minutes of the PGT.
  • time limit test at MAS (conducted after 15 min of having completed the PGT)
Read the detailed description

Aim:

To analyse and compare the acute effect of two different nitrate formulations on strength and endurance performance in young recreationally trained individuals. In a cross-over within-participant comparison design the participants will be assigned either to ingest (i) 600 mg of Nitrate (N), ii) 600 mg Nitrate and Citrulline (NC) and (iii) Placebo (PL).

Design: Cross-over randomised controlled within participant design including one group undertaking three different treatment conditions.

  1. Nitrate (N) providing 600 mg (9.6 mmol) of Nitrate (NO-3).
  2. Nitrate + Citrulline (NC) providing 600 mg (9.6 mmol) of Nitrate (NO-3) and 6 g of citrulline-malate.
  3. Placebo (PLA) Participants (15 or higher) Inclusion criteria: (a) males and females 18-40 years of age; (b) physically active participants with experience in resistance training performing squat and endurance running as habitual exercises (c) free from musculoskeletal limitations or injuries, (d) agree not to ingest any other supplement during the study.

Exclusion criteria: (a) a history of various metabolic conditions or diseases; (b) use of a variety of medications, including but not limited to those with androgenic and/or anabolic effects and/or nutritional supplements known to affect training outcomes such as creatine, proteins, etc. within 6 weeks before the beginning of the study, (c) current use of tobacco products.

All participants must provide written informed consent by the Declaration of Helsinki. The University ethics committee must approve procedures before starting with the data collection.

Procedures Day 0: Familiarization with the testing procedures including the progressive test to determine the 1RM value in Squat.

Diet Record: Each participant will complete a 1-week diet record using a food frequency questionnaire (FFQ). This questionnaire consists of questions relating to the weekly consumption of different types of food, to estimate energy consumption and the nutritional composition of the reported diets. Participants were instructed to maintain their habitual diet throughout the study. If any change in diet patterns is identified, the participants were dropped from the study.

Supplementation protocol:

Days 1 to 3 Supplements (N, NC, or PLA) will be ingested 2 hr before a standard low-volume training session including 3 sets of 8 to 10 reps of squat and deadlift using a very light load (e.g., own body mass), and flexibility exercises following by 5 min of running at self-paced intensity rated as light (RPE 12). This routine can be completed at home.

Day 4: supplements will be ingested 2.5 hours before the assessments.

The three conditions Nitrate (N) Nitrate + Citrulline (NC) and Placebo (PL) will be tested one week apart, considering a minimum washout period of 72 hours, a strategy that has previously been used in studies with a similar design.

All participants will be following an identical training week in each of the three treatment conditions.

Dependent variables:

o Number of completed repetitions in a singular set to failure in a squat with 75% of 1RM.

Lactate Post (within 1 min of having completed the squat) 15 min rest Progressive to exhaustion on a treadmill (PGT)

  • Ventilatory thresholds (VT1) and (VT2)
  • Vo2 max
  • Lactate post (within 1 min of having completed the PGT)
  • Rating of perceived exertion (RPE) using the Borg 6-to-20-point scale recorded every 2 min and at the end of the PGT.
  • Heart rate associated with VT1, VT2, and Vo2max - Heart rate maximum.
  • Maximal aerobic speed (MAS): calculated from the average speed of the last 2 minutes of the PGT.

    15 min rest

  • Maximal Aerobic Speed test (no cortex).
  • Lactate pre (15 min post PGT)
  • The participants should run until exhaustion at the previously determined MAS (e.g. 19.8 km/h)
  • RPE after 1 minute and at the end
  • Heart rate every 1 minute and at the end
  • Lactate post (within 1 minute of having completed the test
02

Conditions studied

  • Nitrate
  • Nitrate/Citrulline
  • Placebo
03

In context

Lead sponsor

University of Greenwich is the lead sponsor of 10 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Physically active participants with experience in resistance training performing squats and endurance running as habitual exercises
  • Free from musculoskeletal limitations or injuries
  • Agree not to ingest any other supplement during the study.

Exclusion criteria

Exclusion Criteria

  • History of various metabolic conditions or diseases
  • Use of a variety of medications, including but not limited to those with androgenic or anabolic effects or nutritional supplements known to affect training outcomes such as creatine, proteins, etc. within 6 weeks before the beginning of the study
  • Current use of tobacco products.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
15 participants (actual)

Study arms

  • Experimental
    Nitrate

    A gel providing 600 mg (9.6 mmol) of nitrate.

    Dietary Supplement: Nitrate

  • Experimental
    Nitrated and citrulline

    A gel, providing 600mg of nitrate (9.6 mmol) and 6 g of citrulline-malate

    Dietary Supplement: Nitrate

  • Placebo comparator
    Placebo

    Placebo in gel format providing negligible amount of nitrate

    Dietary Supplement: Nitrate

Interventions

  • Dietary supplementNitrate

    A four-day supplementation period, separated by one week including a 3-day washout period between conditions will be applied before conducting strength and endurance assessments Days 1 to 3 the randomly assigned supplement (N, NC, or PLA) will be ingested 2 hr before a standard low-volume training session including 3 sets of 8 to 10 reps of squat and deadlift using a very light load (e.g., own body mass) and flexibility exercises following by 5 min of running at self-paced intensity rated as light (12) with the rating of perceived exertion Borg Scale. Day 4: the assigned supplement will be ingested 2.5 h before the assessments Assessment of strength and endurance will be conducted

    Also known as: Nitrated and citrulline, Placebo

06

What researchers measure

Primary outcomes

  1. Strength

    Ten maximum repetitions set in back squat using 75% of the previously determined maximal strength determined by the maximum amount of kg lifter in one sigulare repetitions

    Time frame: Day 4, 2.5 hours after ingesting the supplement

  2. Maximum oxygen consumption (Vo2max)

    The highest level of oxygen determined during a progressive to exhaustion running test on a treadmill (PGT)

    Time frame: through study completion up to 3 weeks

Secondary outcomes

  1. Ventilatory thresholds (VT1) and (VT2)

    ventilatory thresholds using a gas analyser during a progressive to exhaustion running test on a treadmill (PGT)

    Time frame: 15 minutes after completing the strength test

  2. lactate

    lactate concentration

    Time frame: through study completion up to 3 weeks

  3. Heart Rate

    Heart Rate response to endurance PGT test

    Time frame: through study completion up to 3 weeks

  4. Rate of Perceived Exertion

    Perception of effort

    Time frame: through study completion up to 3 weeks

Other outcomes

  1. Maximal Aerobic Speed

    the speed at which the Vo2 maximum is determined during the PGT test

    Time frame: through study completion up to 3 weeks

07

Study locations

1 site
  • Sparrows Farm
    Eltham, London SE9 2BT, United Kingdom
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06531070
Lead sponsor
University of Greenwich
Collaborators
Crown Sport Nutrition
Responsible party
Fernando Naclerio (Professor, University of Greenwich) — Principal investigator
First posted
Jul 31, 2024
Start date
Aug 1, 2024
Primary completion
Oct 15, 2024
Completion
Dec 15, 2024
Last update
Mar 27, 2025

Study contacts

Fernando Naclerio
principal investigator · University of Greenwich

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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