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RECRUITING NA

Effect of Resveratrol Supplementation on Exercise Performance and Recovery

NCT06723119 · View on ClinicalTrials.gov ↗

Study Summary

To examine the effects of once daily supplementation with 500mg VeriSperse® resveratrol (VRES) for 17 days on muscle function, delayed onset muscle soreness, systemic concentrations of muscular damage markers and markers of oxidative stress in resistance trained young adult males following a damaging isoinertial squat protocol (ISP).

Interventions

  • OTHER Resveratrol (VRES) 500 mg oral once daily.
  • OTHER Placebo 500 mg oral once daily.

Study Locations (1)

Florida

  • University of Central Florida EPIC Lab — Orlando

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-10-01
Est. Completion 2025-04-01
Phase NA

Sponsor

University of Central Florida

189 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06723119

The ClinicalTrials.gov registry entry for NCT06723119 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Central Florida, which has 189 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Effect of Resveratrol on Performance and Recovery appearing as the primary indexed condition, and to 2 interventions — of which Resveratrol (VRES) 500 mg oral once daily. is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06723119 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06723119 about?

NCT06723119 is a clinical study titled "Effect of Resveratrol Supplementation on Exercise Performance and Recovery". To examine the effects of once daily supplementation with 500mg VeriSperse® resveratrol (VRES) for 17 days on muscle function, delayed onset muscle soreness, systemic concentrations of muscular damage markers and markers of oxidative stress in resistance trained young adult males following a damagin...

What is the current status of trial NCT06723119?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2024-10-01. Estimated completion is 2025-04-01.

What conditions does trial NCT06723119 study?

This clinical trial studies the following conditions: Effect of Resveratrol on Performance and Recovery. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06723119?

The interventions under investigation include: Resveratrol (VRES) 500 mg oral once daily. (OTHER), Placebo 500 mg oral once daily. (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06723119?

This trial is sponsored by University of Central Florida, which has 189 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06723119 being conducted?

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

Related

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