Postprandial Response to Fruit Juice

Part of paid clinical trials in Addison, Illinois.

Sponsor
Ocean Spray Cranberries, Inc.
Study ID
NCT07103083
Status
Recruiting
Apply to this trial

Conditions

  • Blood Glucose
  • Blood Insulin

Eligibility Criteria

Sex
ALL
Age
18 Years - 45 Years
Healthy Volunteers
Accepted

Interventions

  • Beverage 1 — DIETARY_SUPPLEMENT
    Fruit juice with zero sugar
  • Beverage 2 — DIETARY_SUPPLEMENT
    Fruit juice with low sugar - formulation 1
  • Beverage 3 — DIETARY_SUPPLEMENT
    Fruit juice with low sugar - formulation 2
  • Beverage 4 — DIETARY_SUPPLEMENT
    Fruit juice with full sugar
  • Beverage 5 — DIETARY_SUPPLEMENT
    Fruit juice with full sugar
  • Beverage 6 — DIETARY_SUPPLEMENT
    Glucose control beverage

Study Details

The goal of this clinical trial is to determine postprandial responses to fruit juices.

Key Dates

Start date
Jul 21, 2025
Status verified
Jul 2025
Primary completion
Sep 26, 2025
Completion
Oct 29, 2025

Study Design

Enrollment
18 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT

Arms

  • Experimental: First product order: order not stated to protect study blinding
    Participant will receive each of the 6 study products sequentially in a cross-over design, consuming one study product for one visit, followed by 3-7-day wash-out period before beginning the next product in the sequence.
  • Experimental: Second product order: order not stated to protect study blinding
    Participant will receive each of the 6 study products sequentially in a cross-over design, consuming one study product for one visit, followed by 3-7-day wash-out period before beginning the next product in the sequence.
  • Experimental: Third product order: order not stated to protect study blinding
    Participant will receive each of the 6 study products sequentially in a cross-over design, consuming one study product for one visit, followed by 3-7-day wash-out period before beginning the next product in the sequence.
  • Experimental: Fourth product order: order not stated to protect study blinding
    Participant will receive each of the 6 study products sequentially in a cross-over design, consuming one study product for one visit, followed by 3-7-day wash-out period before beginning the next product in the sequence.
  • Experimental: Fifth product order: order not stated to protect study blinding
    Participant will receive each of the 6 study products sequentially in a cross-over design, consuming one study product for one visit, followed by 3-7-day wash-out period before beginning the next product in the sequence.
  • Experimental: Sixth product order: order not stated to protect study blinding
    Participant will receive each of the 6 study products sequentially in a cross-over design, consuming one study product for one visit, followed by 3-7-day wash-out period before beginning the next product in the sequence.

Primary Outcome Measure

Blood glucose iAUC - 2 hours [ Time Frame: 2 hours ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Biofortis Innovation ServicesAddisonIllinois60101
Kristen Taggart
[email protected]
630-330-0463
Elizabeth Antoo, MD (PRINCIPAL_INVESTIGATOR)

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By research site
Biofortis Innovation Services· Addison, IL

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