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NCT04790552: FastBar2

Effects of Fast Bar on Intermittent Fasting

Completed NA Last updated 9 September 2021
What this trial tests

NA trial testing Dinner in Fasting in 89 participants. Completed in 14 August 2021.

Timeline
1 March 2021
Primary endpoint
1 August 2021
14 August 2021

Quick facts

Lead sponsorL-Nutra Inc
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment89
Start date1 March 2021
Primary completion1 August 2021
Estimated completion14 August 2021
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

L-Nutra Inc

Who can join

Adults 18 to 65, any sex, with Fasting. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates how Fast Bar(TM), a specially formulated energy bar, when consumed with coffee or tea, affects the physiological condition in participants after an overnight fasting. Participants will fast for 19 hours (Fast Group), consume a Fast Bar in the night (Night Bar Group) or in the morning (Bar+Coffee and Bar+Tea Groups) after an approximately 15-hour overnight fasting. Participants will be assessed for physiological parameters associated with fasting.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A Novel Approach to Maintain Physiological Ketosis During Intermittent Fasting With the Consumption of a Fast BarTM and Coffee or Tea: a Randomized, Controlled Study
    · 2022

Verify or expand the search:

Other trials of Dinner

Trials testing the same drug.

Other recruiting trials for Fasting

Currently open trials in the same condition.

Other L-Nutra Inc trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04790552.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing