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NCT05869110Completed

OLFactory Odour Stimulation and FOOD Preferences

OLFO-FOOD: OLFactory Odour Stimulation and FOOD Preferences

Source: ClinicalTrials.gov · Last updated 12 Dec 2024

Brief summary (registry, in English)

The aim of the present "OLFO-FOOD" clinical trial is to investigate, if olfactory stimulation impacts food choice, reference and calorie intake in humans with obesity assessed using a test buffet.

Status (registry)
Completed
Study type
Interventional
Enrollment
24 (actual)
First submitted
11 May 2023
Start date
20 Apr 2023
Primary completion date
31 Jul 2024
Lead sponsor
University Hospital, Basel, Switzerland
Diseases
Obesity
NCT number
NCT05869110

What you commit to

  • Study type: Interventional
  • Participants enrolled: 24
  • From 20 Apr 2023 to the primary completion date, 31 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Surgical intervention of the nasal cavity or the paranasal sinus
  • Current illicit drug abuse including daily marijuana and CBD (Cannabidiol) consumption (alcohol ≤2 drinks per day allowed)
  • Treatment with insulin-sensitizing drugs within the last 3 months
  • Treatment with Glucagon-like Peptide 1 (GLP1)-analoga
  • Regular use of psychopharmaceutic drugs
  • Bariatric surgery

Other illness

  • Known allergy to olfactory stimulation substance, citrus fruits, citrus flavours, citrus food products
  • Lactose-intolerance, celiac disease or non-celiac wheat sensitivity
  • Eating disorder (now or in the past)
  • Acute disease affecting food intake
  • Acute upper respiratory tract infection, acute or chronic sinusitis
  • Severe visual impairment (vision \<10%)
  • Any kind of severe chronic disease (e.g. severe heart failure, active cancer disease)
  • Type 1 and 2 diabetes mellitus
  • History of neurodegenerative diseases, severe head trauma
  • Severe renal impairment (e.g. estimated glomerular filtration rate \<30 ml/min/m2)
  • Known liver cirrhosis or other severe liver impairment
  • Uncontrolled hypertension
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.

Other

  • Diet other than omnivore or vegetarian
  • Dysphagia
  • Use of any kind of decongestant more than twice a week
  • Uncontrolled dysthyroidism
  • Study participants aims to start a new diet or exercise program during the study
  • Pregnancy/Lactation
  • Participation in an interventional study within the last 3 months

Who the study is looking for

  • Age 18-60 years
  • Written informed consent
  • BMI ≥30 kg/m2
  • Normosmia (as defined by Sniffin' Sticks Test)

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.