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

NCT02335008 · ClinicalTrials.gov registry record · NA

The Effect of Artificial Sweeteners (AFS) on Sweetness Sensitivity and Preference - Pilot

A NA study, sponsored by Yale University.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT02335008: Completed NA study, sponsored by Yale University.

NCT02335008 is a NA study that has completed, run by Yale University. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02335008, a NA study, has completed, sponsored by Yale University.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

The goal of this study is to test the hypothesis that repeated consumption of artificial sweetener reduces sweet taste intensity.

Primary Outcome

general labeled magnitude scale ratings of taste intensity

Interventions

  • DIETARY_SUPPLEMENT Sucrose
  • DIETARY_SUPPLEMENT Sucralose

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2014-09
Est. Completion 2015-07
Phase NA
Yale University

1,492 total trials

What the finished NCT02335008 record still lists

NCT02335008 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Sucrose is the first listed.

NCT02335008 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02335008 about?

NCT02335008 is a clinical study titled "The Effect of Artificial Sweeteners (AFS) on Sweetness Sensitivity and Preference - Pilot". The goal of this study is to test the hypothesis that repeated consumption of artificial sweetener reduces sweet taste intensity.

What is the current status of trial NCT02335008?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2014-09. Estimated completion is 2015-07.

What interventions are being tested in trial NCT02335008?

The interventions under investigation include: Sucrose (DIETARY_SUPPLEMENT), Sucralose (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT02335008?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02335008's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

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 NCT02335008, the US trial registry maintained by the National Library of Medicine. NCT02335008 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.