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NCT06544954 · ClinicalTrials.gov registry record · NA

Prebiotic Effects of California Grapes on Gut Health and Cardiometabolic Health in Overweight Men and Women

A NA study of Inflammation and Blood Pressure, sponsored by University of California, Davis.

Recruiting
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT06544954: Recruiting NA study of Inflammation and Blood Pressure, sponsored by University of California, Davis.

NCT06544954 is a NA study of Inflammation and Blood Pressure that is actively recruiting participants, run by University of California, Davis. The registered enrollment target is 40 participants, below the 288-participant average among 132 other Inflammation trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06544954, a NA study of Inflammation and Blood Pressure, is actively recruiting participants, sponsored by University of California, Davis.

RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to assess the impact of table grape consumption on gut microbiome, intestinal permeability, systemic inflammation, and vascular function in healthy overweight men and women aged 45-70 years. The main questions it aims to answer are: * Does daily grape intake alter intestinal microbiome composition and intestinal permeability? * Are changes in gut microbiota and intestinal permeability correlated with changes in cardiometabolic risk factors (inflammation, vascular function, lipid profiles)? * Does response to grape intake on gut microbiota, intestinal permeability, cardiometabolic and inflammatory markers differ between men and women? * Are metabolic pathways modified by grape consumption able to explain the link between gut health and cardiometabolic factors? Researchers will compare freeze-dried grape powder to placebo powder to see if grape powder improves cardiometabolic risk factors. Participants will * Consume the powder dissolved in water twice daily for 3 weeks * Follow their usual diet, modified to limit polyphenol-rich foods * Visit the clinic at the beginning and end of the intervention for vascular measurements and blood sample collection * Complete a 3-day 24-hour dietary recall and collect stool sample before each visit

Primary Outcome

Pulse Wave Velocity (PWV) from carotid to femoral artery after 5 minutes rest; PWV is an established index of aortic stiffness using a validated non-invasive device that allows online pulse wave recording and automatic PWV calculation

Interventions

  • OTHER Placebo powder
  • DIETARY_SUPPLEMENT Freeze-dried grape powder

Study Locations (1)

California

  • Ragle Human Nutrition Center - Davis

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2024-12-02
Est. Completion 2026-01
Phase NA
University of California, Davis

657 total trials

What NCT06544954 shows while recruiting

NCT06544954 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 288-participant average among 132 other Inflammation trials with a reported enrollment target (86% lower).

The record links to 5 conditions, with Inflammation appearing as the primary indexed condition, and to 2 interventions - of which Placebo powder is the first listed.

NCT06544954 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06544954 about?

NCT06544954 is a clinical study titled "Prebiotic Effects of California Grapes on Gut Health and Cardiometabolic Health in Overweight Men and Women". The goal of this clinical trial is to assess the impact of table grape consumption on gut microbiome, intestinal permeability, systemic inflammation, and vascular function in healthy overweight men and women aged 45-70 years. The main questions it aims to answer are: * Does daily grape intake alter...

What is the current status of trial NCT06544954?

This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2024-12-02. Estimated completion is 2026-01.

What conditions does trial NCT06544954 study?

This clinical trial studies the following conditions: Inflammation, Blood Pressure, Dysbiosis, Arterial Stiffness, Permeability; Increased.

What interventions are being tested in trial NCT06544954?

The interventions under investigation include: Placebo powder (OTHER), Freeze-dried grape powder (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT06544954?

This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06544954 being conducted?

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

Similar trials for Inflammation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06544954's enrollment target sits among peer trials

40 83rd of 132 higher than 46 of 132 other Inflammation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Inflammation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06544954, the US trial registry maintained by the National Library of Medicine. NCT06544954 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.