NCT07147010

Brief Summary

The goal of this study is to evaluate correlations between VOCs in the breath and venous blood glucose values in various glycaemic states in people living with Type 2 Diabetes. VOCs are measured with a gold-standard GC-IMS device and a prototype of a novel breath analyzer. Participants will be exposed to different blood glucose levels at different rates of change by administering glucose solution and insulin and by a meal challenge.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable type-2-diabetes

Timeline
Completed

Started Oct 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

August 21, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 28, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 27, 2025

Completed
Last Updated

December 9, 2025

Status Verified

December 1, 2025

Enrollment Period

6 months

First QC Date

August 21, 2025

Last Update Submit

December 2, 2025

Conditions

Keywords

Volatile Organic CompoundsGlucose excursionsRates of change of glucose valuesHyperglycaemiaHypoglycaemiaGas Chromatography - Ion Mobility SpectrometryEuglycaemiaBreath-analysis

Outcome Measures

Primary Outcomes (1)

  • VOC spectra

    Primary outcome focuses on VOC spectra (measured with the GC-IMS) across varying intravenous blood glucose levels

    6-8 hour study visit

Secondary Outcomes (5)

  • Inter-Participant VOC Variability

    6-8 hour study visit

  • Intra-Participant VOC Variability

    6-8 hour study visit

  • MIB VOC Spectra Analysis

    6-8 hour study visit

  • VOC Spectra Response Time

    6-8 hour study visit

  • Comparison of meal vs clamp induced VOC changes

    6-8 hour study visit

Study Arms (1)

People with Type 2 Diabetes

EXPERIMENTAL

Exposure to various glycaemic states at different rates of change by administering glucose solution, insulin, or a standardized meal.

Device: MIB Breath Analyzer

Interventions

Going through visit-specific blood glucose excursions by the administration of glucose and insulin (clamp), monitoring physiological processes, and measuring reference blood glucose values and VOC measurements in the breath using a GC-IMS and the MIBs (investigational devices). Going through visit-specific blood glucose excursions by consuming a standardized meal, monitoring physiological processes, and measuring reference blood glucose values and VOC measurements in the breath using a GC-IMS and the MIBs (investigational devices) Imitating the glucose excursion from the meal excursion by infusing glucose and insulin (clamp), monitoring physiological processes, and measuring reference blood glucose values and VOC measurements in the breath using a GC-IMS and the MIBs (investigational devices).

Also known as: GC-IMS as gold standard
People with Type 2 Diabetes

Eligibility Criteria

Age45 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Signed written informed consent
  • T2D treated with one or more oral anti-diabetic drugs (incl GLP-1 and/or GIP)
  • \< 10 years since T2D diagnosis
  • HbA1c ≤8% (HbA1c based on last measurement by treating physician but not older than 120 days)
  • Willingness to undergo study procedures
  • Age 45 -70 years (inclusive)

You may not qualify if:

  • Pregnancy and/or lactation period
  • Currently on chronic or occasional treatment with pulmonary drugs
  • Insulin dependency
  • Smoking (last cigarette within the last six months)
  • BMI above 30 kg/m²
  • Lp(a) above 125 nmol/l
  • LDL not in the individual target range of an earlier cholesterol goal according ESC guideline 2021 (LDL based on last measurement by treating physician but not older than 30 days)
  • Irregular 12-lead ECG or increased carotid plaque burden based on a three-point sonography. Both examinations are performed and evaluated according to the investigator's judgment.
  • History of, or manifested, cardiovascular diseases
  • Medical history of epilepsy or other neurological disease associated with seizure events
  • Known sensitivity to medical grade adhesives
  • Comorbidities that are suspected to alter the VOC spectra
  • Participation in another investigation with an investigational drug within the 30 days preceding and during the present investigation
  • Not able to understand, write or read German

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Inselspital Bern

Bern, 3010, Switzerland

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 2HyperglycemiaHypoglycemia

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System Diseases

Study Officials

  • Frank Flacke, Dr.

    BOYDSense SAS

    STUDY CHAIR
  • Markus Laimer, Dr. med

    Inselspital Bern, Switzerland

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: The intervention consists of inducing different glycaemic states in people with diabetes.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 21, 2025

First Posted

August 28, 2025

Study Start

October 1, 2024

Primary Completion

March 30, 2025

Study Completion

November 27, 2025

Last Updated

December 9, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

There is no plan to share data regarding the main aims of the study.

Locations