Drinkometer reveals secrets of Post-Surgery eating
NCT ID NCT06538948
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tracks 420 people to see how bariatric surgery affects drinking behavior using a special device called a drinkometer. It measures things like sip size and speed, and looks at how gut hormones and sex differences play a role. The goal is to better understand why surgery helps with weight loss, beyond what people report about their eating habits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could reveal how bariatric surgery changes eating behavior, helping improve long-term weight loss outcomes.
- What could go wrong
- This is an observational study, not a treatment trial. It may not find clear links between drinking patterns and hormones or weight loss.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 420 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants with obesity and scheduled for bariatric surgery are recruited consecutively at the outpatient clinic of bariatric surgery at the University Hospital Zurich. Participants with obesity not scheduled for surgery are recruited at the private clinic "Adimed" in Winterthur. Participants without obesity are recruited from students, employees and faculty of the Faculty of Medicine of the University of Zurich.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 year * BMI ≥ 35 kg/m2 for patients with planned RYGB or SG operation * BMI ≥ 30 kg/m2 for external controls affected by obesity but no planned RYGB or SG within the next 12 months, and * BMI ≥ 18.5 kg/m2 and ≤ 24.9 kg/m2 for controls without obesity. Exclusion Criteria: * history of previous bariatric operations and/ or revisional surgery (e.g., alteration of limb lengths after primary RYGB), * smoking, * established diagnosis of type 1 or 2 diabetes mellitus, and * polycystic ovary syndrome (PCOS).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Männedorf
RECRUITINGMännedorf, Canton of Zurich, 8708, Switzerland
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University Hospital Zurich, Department of Surgery and Transplantation
RECRUITINGZurich, Canton of Zurich, 8091, Switzerland
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Other studies related to the condition(s) this trial covers.
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- Can a cold cloth on the neck calm Post-Surgery nausea?