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Taking people in SwitzerlandEarly phase 1

Tests whether an inhaled natural odour reaches spinal fluid in people with obesity

Tests an inhaled natural odour in adults with overweight or obesity, and in lean adults.

Plain-language title generated from the registry record
Registry title: ABUNDANCE of A NATURAL ODOUR in HUMAN CEREBROSPINAL FLUID AFTER OLFACTORY EXPOSURE - the OLFO-Brain Study

Key facts

Where
Basel, SwitzerlandSee the 2 sites
Phase
Early phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 60 years old?

Source: NCT06370845, who can take part

Where in Switzerland

  • University Hospital BaselBasel, SwitzerlandNot yet recruiting
  • University Hospital of BaselBasel, SwitzerlandTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT06370845
Record updated
4 May 2026
Original description
The goal of this clinical trial is to investigate the abundance of a natural odour in human cerebrospinal fluid in obese and lean participants after inhalation thereof. Participants will undergo blood sample collection and inhalation of either a natural odour or placebo through an inhaler in addition to a liquor puncture prescribed in standard of care context.Read full original descriptionShow less

Abundance of a Natural Odour in Human Cerebrospinal Fluid After Olfactory Exposure - the OLFO-Brain Study

The goal of this clinical trial is to investigate the abundance of a natural odour in human cerebrospinal fluid in obese and lean participants after inhalation thereof. Participants will undergo blood sample collection and inhalation of either a natural odour or placebo through an inhaler in addition to a liquor puncture prescribed in standard of care context.

Inclusion: Age 18-60 years; Written informed consent; Scheduled for routine liquor puncture; BMI ≥ 30 kg/m2; No proven diagnose of diabetes; Age 18-60 years; Written informed consent; Scheduled for routine liquor puncture; BMI 18-25 kg/m2.

Exclusion: Present or past surgical intervention of the nasal cavity, the paranasal sinus, the pituitary or the frontal brain; Known allergy to the natural odour; Acute upper respiratory tract infection, acute or chronic sinusitis; Any kind of severe chronic disease (e.g. severe heart failure, active cancer disease, severe renal impairment with an estimated glomerular filtration rate <30 ml/min/m2); Pregnancy/lactation; Inability to understand the study procedure and to sign the study consent.

ClinicalTrials.gov NCT06370845