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NCT04498455 · ClinicalTrials.gov registry record · Phase 4

Study of a Prebiotic Supplement to Mitigate Excessive Weight Gain Among Physicians in Residency

A Phase 4 study of Metabolic Syndrome and Weight Gain Trajectory, sponsored by Baylor University.

Completed
Registry status
Phase 4
Development phase
11
Enrollment target
1
Study location

NCT04498455 is a Phase 4 study of Metabolic Syndrome and Weight Gain Trajectory that has completed, run by Baylor University. The registered enrollment target is 11 participants, below the 1,205-participant average among 102 other Metabolic Syndrome trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04498455, a Phase 4 study of Metabolic Syndrome and Weight Gain Trajectory, has completed, sponsored by Baylor University.

COMPLETED
Registry status
Phase 4
Development phase
11 participants
Enrollment target
1
Study location

Study Summary

A randomized placebo controlled trial to determine if increased dietary fiber will prevent weight gain, inhibit adiposity and reduce perceived stress levels in residents at the Waco Family Health Center as the result of changes in distal gut microbiota composition and function.

Interventions

  • DIETARY_SUPPLEMENT Prebiotin

Study Locations (1)

Texas

  • Baylor University - Waco

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2018-09-30
Est. Completion 2019-02-15
Phase Phase 4

Sponsor

Baylor University

33 total trials

What the Registry Record Tells You About NCT04498455

The ClinicalTrials.gov registry entry for NCT04498455 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,205-participant average among 102 other Metabolic Syndrome trials with a reported enrollment target (99% lower). The listed sponsor is Baylor University, which has 33 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Metabolic Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Prebiotin is the first listed.

NCT04498455 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT04498455 about?

NCT04498455 is a clinical study titled "Study of a Prebiotic Supplement to Mitigate Excessive Weight Gain Among Physicians in Residency". A randomized placebo controlled trial to determine if increased dietary fiber will prevent weight gain, inhibit adiposity and reduce perceived stress levels in residents at the Waco Family Health Center as the result of changes in distal gut microbiota composition and function.

What is the current status of trial NCT04498455?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 11 participants. The study started on 2018-09-30. Estimated completion is 2019-02-15.

What conditions does trial NCT04498455 study?

This clinical trial studies the following conditions: Metabolic Syndrome, Weight Gain Trajectory.

What interventions are being tested in trial NCT04498455?

The interventions under investigation include: Prebiotin (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT04498455?

This trial is sponsored by Baylor University, which has 33 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04498455 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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