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Influence of Salbutamol on Emotional and Cognitive Functions in Healthy Subjects

Influence of Salbutamol on Emotional and Cognitive Functions in Healthy Subjects

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01957293
Acronym
Salmon-Basel
Enrollment
40
Registered
2013-10-08
Start date
2013-10-31
Completion date
2014-02-28
Last updated
2014-12-16

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

Conditions

Memory Functions

Brief summary

Aim is to investigate the effect of beta2 adrenergic stimulant salbutamol on emotional and cognitive functions in healthy humans.

Interventions

DRUGSalbutamol

single oral administration, 4 mg

DRUGPlacebo

single oral administration

Sponsors

Clinical Trial Unit, University Hospital Basel, Switzerland
CollaboratorOTHER
Prof. Dominique de Quervain, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy, male and female, aged between 18 and 40, BMI be-tween 19 and 27 kg/m2, normotensive (BP between 90/60 mmHg and 140/90 mmHg), native or fluent German-speaking, caucasian (European ancestry), able and willing to give written informed consent and comply with the requirements of the study protocol, willing to donate saliva sample for DNA-analysis -

Exclusion criteria

Acute or chronic psychiatric or somatic disorder, tachycardia at rest (\> 100 bpm), known hypersensitivity to salbutamol, pathological ECG, pregnancy, breast-feeding, long-term medication within last 3 months (oral contraceptives are disregarded) smoking (\>3 cigarettes per day), concurrent participation in another study, participation in one of our previous studies using the same memory tests, inability to read and understand the participant's information. -

Design outcomes

Primary

MeasureTime frameDescription
Change of emotional memory functions under Salbutamoltwo testing days within 10 daysmemory tests
Change of episodic memory functions under Salbutamoltwo testing days within10 daysmemory tests

Secondary

MeasureTime frameDescription
Change of emotional state under salbutamolTwo testing days within 10 daysquestionnaires
change of attention functions under salbutamoltwo testing days within 10 daysattention tests

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026