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CompletedNCT03548038Updated Nov 2, 2020

Taste Changes With Bariatric Surgery

An observational study in Taste, Altered, sponsored by University of Missouri-Columbia. Completed at 2 sites in United States. Open to female participants aged 21 Years to 70 Years. Per ClinicalTrials.gov, last updated 2020-11-02.

Sponsored by University of Missouri-Columbia · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
21
Ages
21 Years to 70 Years
Sex
Female
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Study summary

It is commonly believed that a link exists between BMI and taste perception. One group of researchers observed that women who are obese experience reduced taste sensitivity when compared to normal-weight controls. Others have compared taste sensitivity between lean and obese subjects and found no significant differences. The inconsistencies in these studies demonstrate how much variation in taste sensitivity is possible when different factors are applied in research. Throughout several studies, one element remains constant - bariatric surgery causes appetite aversions. These changes in appetite and food preference likely have a large influence on the overall magnitude of post-surgical weight loss. Although many studies have investigated the changes in taste preference after bariatric surgery, few, if any, have focused on changes in sweet taste perception.

Read the detailed description

The overall goal of the present project is to determine how future bariatric surgery will affect the taste for sweet liquids. Taste perception will be assessed before surgery (pre-operative, pre-op) and after bariatric surgery, at approximately 1 month. Taste studies will be conducted with solutions prepared freshly before each test using sucrose dissolved in distilled water. Six concentrations of sucrose (table sugar) will be tasted in random order, with the most concentrated solution being roughly the sweetness of soda. The subject is blinded to the concentrations. It is hypothesized that there will be no significant difference in taste perception when pre-op and post-op values are compared. However, the investigators hypothesize that taste preference will identify solutions with lower concentrations post-op.

02

Conditions studied

  • Taste, Altered

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Keywords

  • taste perception
  • bariatric surgery
  • taste preference
  • weight loss surgery
03

In context

Dysgeusia

52 studies on the registry are indexed under Dysgeusia; 12 are open to participants now.

This study's enrollment of 21 is below the median of 104 across 22 observational studies indexed under Dysgeusia.

Browse Dysgeusia studies →

Lead sponsor

University of Missouri-Columbia is the lead sponsor of 365 studies on the registry; 69 are open to participants now.

Of its 43 completed or terminated interventional studies of FDA-regulated products, 29 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 70 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Women aged 21-70 will be recruited from the University of Missouri Bariatric Surgery Clinic.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Women who plan to undergo bariatric surgery.
  • Age: 21-70y.
  • Non-smokers (at least 3 months post smoking cessation).
  • Non-diabetic or prediabetic

Exclusion criteria

Exclusion Criteria:

  • Subject on a medication known to affect taste perception: Antibiotics, thyroid medications, psychotropic, neurological, and cardiac medications.
  • Inability to understand the test instructions.
  • Subject has already undergone bariatric surgery
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
21 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Bariatric surgery patients

    All subjects will be patients scheduled for bariatric surgery. There is only one arm in this study.

    Other: taste test

Interventions

  • Othertaste test

    All subjects will complete a procedure to determine their taste sensitivity to sweet tastants.

06

What researchers measure

Primary outcomes

  1. Taste Perception on an Interval Scale

    Taste perception will be assessed by the subjects' responses to varying sucrose solutions. The interval scale begins with "barely detectable" at zero and goes up to "strongest imaginable" at 10. Subjects will be asked to draw an "X" at the location on the graph corresponding to their perception.

    Time frame: Change from baseline to one month after bariatric surgery

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Study locations

2 sites
  • Elizabeth Parks
    Columbia, Missouri 65212, United States
  • University of Missouri
    Columbia, Missouri 65212, United States
08

References and documents

Publications

  • Bueter M, Miras AD, Chichger H, Fenske W, Ghatei MA, Bloom SR, Unwin RJ, Lutz TA, Spector AC, le Roux CW. Alterations of sucrose preference after Roux-en-Y gastric bypass. Physiol Behav. 2011 Oct 24;104(5):709-21. doi: 10.1016/j.physbeh.2011.07.025. Epub 2011 Jul 30. PubMed 21827777 ↗
  • Scruggs DM, Buffington C, Cowan GS Jr. Taste Acuity of the Morbidly Obese before and after Gastric Bypass Surgery. Obes Surg. 1994 Feb;4(1):24-28. doi: 10.1381/096089294765558854. PubMed 10742759 ↗
  • Pepino MY, Finkbeiner S, Beauchamp GK, Mennella JA. Obese women have lower monosodium glutamate taste sensitivity and prefer higher concentrations than do normal-weight women. Obesity (Silver Spring). 2010 May;18(5):959-65. doi: 10.1038/oby.2009.493. Epub 2010 Jan 14. PubMed 20075854 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 2, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03548038
Responsible party
Elizabeth Parks (Professor, University of Missouri-Columbia) — Principal investigator
First posted
Jun 6, 2018
Start date
May 24, 2018
Primary completion
Dec 20, 2019
Completion
May 4, 2020
Last update
Nov 2, 2020

Study contacts

Elizabeth J Parks, PhD
principal investigator · University of Missouri-Columbia

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2020. You cannot join it, but the record below documents what was studied.

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