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Classical conditioning of intranasal insulin in healthy humans

Classical conditioning of intranasal insulin in healthy humans

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
DRKS
Registry ID
DRKS00000537
Enrollment
32
Registered
2010-09-15
Start date
1999-10-07
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

We examined only healthy subjects Application for prevention and treatment of adiposity might be considered

Interventions

Group 1: Intranasally administered insulin (6X 20 international units IU) Group 2: Placebo

Sponsors

Universität Düsseldorf, Klinik für Endokrinologie, Diabetologie und Rheumatologie
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 30 Years

Inclusion criteria

Inclusion criteria: healthy male students

Exclusion criteria

Exclusion criteria: Diabetes (also parents and siblings), allergies, chronic and/or acute rhinitis, diseases and anatomic deviations of the nose, chronic diseases: i.e., cardiovascular disorders; endocrine disorders and neurological diseases, especially seizures, chronic diseases of liver and kidneys, and other chronic diseases; medication with glucocorticoids and psychopharmacological drugs, substance abuse (alcohol, drugs); smoking; athelets were excluded

Design outcomes

Primary

MeasureTime frame
Food-intake behavior (calorie intake) as a reduction in a standardized test meal in the exreimental- compared to the control group; Blood glucose and peripheral insulin under euglycemia: Relative to baseline: cumulative change of blood glucose (11 measurement poits) and insulin (6 measurement points) in the experimental- compared to the control group

Secondary

MeasureTime frame
Peripheral leptin, cortisol, epinephrine, norepinephrine: Cumulative change of the hormones in the experimental- compared to the control group (measurement points see insulin) Memory: Scores in psychometric test (Lern- und Gedächtnistest LGT-3) in the experimental- compared to the control group; EEG: acousticall-evoked potentials in the experimental group compared to the control group (1 measuremnt point baseline, 3 meaurement points during intranasal treatment)

Countries

Germany

Contacts

Public ContactUrsula Stockhorst

Universität Osnabrück Institut für Psychologie Allgemeine Psychologie II und Biologische Psychologie

ursula.stockhorst@uni-osnabrueck.de++49(0)-541-969-4078

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 29, 2026