ClinicalTrials.gov record
Recruiting Not applicable Interventional Accepts healthy volunteers

Dose-Response Impact of Glucosyl-Hesperidin (CitraPeak) on Exercise Performance, Blood Flow, Stress, Cognition, and Other Perceptual Indicators

ClinicalTrials.gov ID: NCT06672952

Public ClinicalTrials.gov record NCT06672952. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 18, 2026, 10:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT06672952
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Lindenwood University
Other
Enrollment
60 participants

Conditions and interventions

Interventions

  • 200 mg CITRAPEAK® (glucosyl-hesperidin) supplementation Dietary Supplement
  • 400 mg CITRAPEAK® (glucosyl-hesperidin) supplementation Dietary Supplement
  • Placebo Dietary Supplement

Dietary Supplement

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 14, 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025
Last update posted
Dec 11, 2025

2025 – 2026

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Lindenwood University Saint Charles Missouri 63301 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06672952, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 11, 2025 · Synced May 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06672952 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →