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Investigation of Benegut® on Immediate GI Discomfort Relief Caused by Acute Overfeeding in Healthy Subjects

NCT05603416 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2023-03-17

No results posted yet for this study

Summary

To determine the relief of GI discomfort after overfeeding with a high caloric meal.

Conditions

  • Healthy Volunteers

Interventions

DIETARY_SUPPLEMENT

Perilla frutescens extract

oral dissolvable powder - dosage 300mg

DIETARY_SUPPLEMENT

Placebo

oral dissolvable powder - dosage 300mg no active ingredient

Sponsors & Collaborators

  • Vital Solutions GmbH

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
25 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-09
Primary Completion
2023-03-02
Completion
2023-04-30

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05603416 on ClinicalTrials.gov