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Clinical Trials/NCT04476238
NCT04476238CompletedNot Applicable

Randomized Cross-over Trial to Investigate the Effect of Inosine on Human Energy Expenditure

University Hospital, Basel, Switzerland1 site in 1 country8 target enrollmentStarted: February 28, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
8
Locations
1
Primary Endpoint
resting energy expenditure after Inosine

Study Overview

Brief Summary

Investigators want to test whether the intake of the nucleoside inosine increases the human energy expenditure. Inosine occurs as a metabolic intermediate in the human body and is sometimes taken as a dietary supplement by athletes.

For this purpose, investigators will measure the basal metabolic rate by indirect calorimetry. Study participants will then take inosine dissolved in water or placebo and energy expenditure will be assessed again.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Healthy male volunteers
  • •BMI between 18-27 kg/m2
  • •Age between 18 and 40 years

Exclusion Criteria

  • •Chronic concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, diabetes mellitus),
  • •Known or suspected non-compliance, drug or alcohol abuse,
  • •Inability to follow the procedures of the study
  • •Participation in another study with investigational drug within the 30 days preceding and during the present study,
  • •Previous enrolment into the current study,
  • •Enrolment of the investigator, his/her family members, employees and other dependent persons,
  • •Thyroid disorders

Arms & Interventions

Water

Placebo Comparator

250 ml of tap water only

Intervention: Placebo (Other)

Inosine

Experimental

2 grams of inosine dissolved in 250 ml of tap water

Intervention: Inosine (Dietary Supplement)

Outcomes

Primary Outcomes

resting energy expenditure after Inosine

Time Frame: one hour after oral intake of inosine

resting energy expenditure (REE) assessed by indirect calorimetry after oral intake of two grams of inosine as compared to placebo

Secondary Outcomes

  • Change in energy expenditure(one hour after oral intake of inosine)
  • Change in Respiratory Quotient(one hour after oral intake of inosine)
  • Serum inosine level(0 hours, 1 hour, 2 hours)

Investigators

Sponsor
University Hospital, Basel, Switzerland
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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