Effects of L-Citrulline or Citrulline-malate on Neuromuscular Performance in Resistance-trained Adults
Malate or Not?: Effects of L-Citrulline or Citrulline-malate on Neuromuscular Performance in Resistance-trained Adults
1 other identifier
interventional
50
1 country
1
Brief Summary
The main aim of this study is to compare the effects of L-Citrulline vs. Citrulline-malate on neuromuscular performance (maximal dynamic strength and maximal endurance strength) in resistance-trained adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 21, 2021
CompletedFirst Posted
Study publicly available on registry
January 11, 2022
CompletedStudy Start
First participant enrolled
February 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2022
CompletedNovember 4, 2022
November 1, 2022
5 months
December 21, 2021
November 3, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Maximal endurance strength
Maximal endurance strength of lower- and upper-body (squat and bench press exercises)
1 hour
Secondary Outcomes (1)
Maximal dynamic strength
1 hour
Study Arms (3)
Experimental: L-Citrulline
EXPERIMENTAL5 g of L-citruline + 5 g of additives. The dose to be administered is that recommended on the labeling and nutritional information of the product, which has been produced under GMP procedures and approved by the EFSA (Lifepro®).
Experimental: Citrulline-malate
EXPERIMENTAL8g of citrulline-malate + 2 g of additives. The dose to be administered is that recommended on the labeling and nutritional information of the products which has been produced under GMP procedures and approved by the EFSA (Lifepro®).
Placebo
PLACEBO COMPARATOR10g of maltodextrin plus additives (Lifepro®).
Interventions
8g of citrulline-malate + 2 g of additives
Eligibility Criteria
You may qualify if:
- Healthy male or female
- Ages 18-30years
- BMI: 18-30.0 kg/m2
- Stable weight over the last 3 months (body weight changes\<3kg)
- Previous experience in resistance training (i.e., at least 1 year with a frequency of two or more training sessions per week),
You may not qualify if:
- History of chronic diseases (renal disease, diabetes, cardiovascular disease, cancer, VIH, hepatic disease, food disorders)
- Pregnant, planning to become pregnant, or breastfeeding
- Have been treated previously or during the study period with prescription drugs:
- antihypertensive, lipid lowering, acid uric lowering, glucose lowering, beta blockers or any drug that under the investigator's judged could influence the results.
- Allergy/intolerance to any ingredient of the dietary supplements.
- Chronic consumers of dietary NO-precursors dietary supplements (citrulline malate, arginine, nitrates).
- Any non-controlled medical condition which could influence results or could be worsened by the participation in the study.
- Are deemed unsuitable by the investigator for any other reason, that prevent data collection.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jonatan Ruiz Ruiz
Granada, 18011, Spain
Related Publications (1)
Martin-Olmedo JJ, Miras-Moreno S, Cuadra-Montes K, Garcia-Ramos A, Ruiz JR, Jurado-Fasoli L. Malate or Not? Acute Effects of L-Citrulline Versus Citrulline Malate on Neuromuscular Performance in Young, Trained Adults: A Randomized, Double-Blind, Placebo-Controlled Crossover Trial. Int J Sport Nutr Exerc Metab. 2024 Dec 11;35(2):89-98. doi: 10.1123/ijsnem.2024-0006. Print 2025 Mar 1.
PMID: 39662304DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Researcher
Study Record Dates
First Submitted
December 21, 2021
First Posted
January 11, 2022
Study Start
February 15, 2022
Primary Completion
June 30, 2022
Study Completion
June 30, 2022
Last Updated
November 4, 2022
Record last verified: 2022-11