Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00661947 · ClinicalTrials.gov registry record

Pharmacokinetics and Pharmacodynamics of Fructose

A clinical trial, sponsored by University of Florida.

Completed
Registry status
40
Enrollment target

NCT00661947: Completed study, sponsored by University of Florida.

NCT00661947 is a clinical trial that has completed, run by University of Florida. The registered enrollment target is 40 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00661947 has completed, sponsored by University of Florida.

COMPLETED
Registry status
40 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether sucrose vs high fructose corn syrup from a soft drink results in differences in various metabolic byproducts such as fructose, glucose, serum uric acid, triglyceride and lactate.

Interventions

  • OTHER Dr Pepper sweetened with sucrose or high fructose corn syrup

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2008-03
Est. Completion 2010-08
University of Florida

1,106 total trials

What the finished NCT00661947 record still lists

NCT00661947 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 40 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Dr Pepper sweetened with sucrose or high fructose corn syrup is the first listed.

NCT00661947 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00661947 about?

NCT00661947 is a clinical study titled "Pharmacokinetics and Pharmacodynamics of Fructose". The purpose of this study is to determine whether sucrose vs high fructose corn syrup from a soft drink results in differences in various metabolic byproducts such as fructose, glucose, serum uric acid, triglyceride and lactate.

What is the current status of trial NCT00661947?

This trial is currently completed. The enrollment target is 40 participants. The study started on 2008-03. Estimated completion is 2010-08.

What interventions are being tested in trial NCT00661947?

The interventions under investigation include: Dr Pepper sweetened with sucrose or high fructose corn syrup (OTHER).

Who is sponsoring clinical trial NCT00661947?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00661947, the US trial registry maintained by the National Library of Medicine. NCT00661947 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.