CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 110 enrolled
Drug / intervention
Dinner +2 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04499599
NCT04499599N/ACompleted
CompareCT.gov

Randomized, Single-blinded, Controlled, Parallel-arm Study to Evaluate the Effect of Fast Bar(TM) on Physiological Fasting Condition

L-Nutra Inc·interventional·Posted Aug 5, 2020·Updated Apr 9, 2024

In Brief

A clinical study evaluating Dinner, Fasting, and 1 other intervention for Fasting. Completed, enrolled 110 participants across 1 site.

Detailed Summary

This study evaluates how Fast Bar(TM), a specially formulated energy bar, affects the physiological condition in participants after an overnight fasting. Participants will fast for 19 hours (Fast Group), consume a breakfast Bar (Breakfast Group) or a Fast Bar(TM) (Fast Bar Group) after an approximately 15-hour overnight fasting. Participants will be assessed for physiological parameters associated with fasting.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsFasting
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedAug 5, 2020
Enrollment StartJul 20, 2020
Primary CompletionSep 28, 2020
Study CompletionSep 30, 2020
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 5.9 years ago

Interventions

Dinnerother

Study subjects will consume a standardized ready-to-eat meal as dinner.

Fastingother

Subjects in all groups will be asked to consume a standardized ready-to-eat dinner meal before 5 pm on day 1 and then fast overnight for approximately 15 hours.

Study foodother

Study subjects will either continue to fast for 6 hours (Fast Group), consume either a breakfast (Breakfast Group) or a Fast Bar (Fast Bar Group).