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NCT04732130: LIMITFOOD

Monitoring During Different Intermittent Fasting Protocols in Non-Obese Adults

Completed NA Last updated 6 October 2023
What this trial tests

NA trial testing Time-Restricted Feeding in Intermittent Fasting in 76 participants. Completed in 1 July 2023.

Timeline
10 March 2021
Primary endpoint
1 July 2023
1 July 2023

Quick facts

Lead sponsorPhilipp Gerber
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment76
Start date10 March 2021
Primary completion1 July 2023
Estimated completion1 July 2023
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Philipp Gerber

Who can join

Adults 18 to 40, any sex, with Intermittent Fasting or Overweight. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

LIMITFOOD is a randomized clinical intervention study that investigates the effects of two different intermittent fasting protocols compared to a control group on the health of normal- and overweight adults. A total of 72 participants will be randomized into three equally sized groups: an alternate day fasting, a time-restricted feeding and a control group.

Publications & conference data

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

  1. Alternate-day fasting elicits larger changes in fat mass than time-restricted eating in adults without obesity - A randomized clinical trial.
    Derron N, Güntner AT, Weber IC, Braun J, et al · · 2025 · cited 2× · PMID 40945487 · DOI 10.1016/j.clnu.2025.08.033

Verify or expand the search:

Other trials of Time-Restricted Feeding

Trials testing the same drug.

Other recruiting trials for Intermittent Fasting

Currently open trials in the same condition.

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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/NCT04732130.

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