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NCT07137988

Effect of Acute Grape Seed Extract Supplementation on the Heart Rate Recovery in Young Individuals

Completed NA Last updated 22 August 2025
What this trial tests

NA trial testing 600 mg grape seed extract in Healthy Young Men in 12 participants. Completed in 31 December 2024.

Timeline
3 October 2024
Primary endpoint
3 December 2024
31 December 2024

Quick facts

Lead sponsorCalifornia Baptist University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposeprevention
Enrollment12
Start date3 October 2024
Primary completion3 December 2024
Estimated completion31 December 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

California Baptist University

Who can join

Adults 18 to 30, male only, with Healthy Young Men. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study hypothesized that sustained sympathoexcitation via MMA slows down PHRR and that GSE supplementation is effective at improving PHRR in young individuals. 12 Participants were randomly assigned, via a double-blind, cross-over design, to either receive GSE (300mg, 2 capsules) or PL (300mg, 2 capsules), with a washout period of at least 72 hrs. between trials. A submaximal exercise test was performed using a cycle ergometer combined with isometric handgrip exercise using a handgrip dynamometer, and blood flow occlusion by placing a cuff over the brachial artery of the dominant arm. Post heart rate recovery (PHRR) was measured at 5 sec. intervals throughout the experiment. The PHRR was evaluated between GSE and PL at every min. for 300 sec.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other California Baptist University trials

Trials by the same sponsor.

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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/NCT07137988.

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