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Differenciated physiological investigation of the effect of exterior applications on healthy subjects - a controlled single blinded clinical trial

Phase 2
Conditions
healthy adults
Registration Number
DRKS00009359
Lead Sponsor
Charité Universitätsmedizin
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Age: 18 to 40
- no physical or mental disease
- written consent

Exclusion Criteria

- severe physical and/or mental disease
- known hypersensitivity towards the used substances
- highly sensitive Skin
- contact allergies or atopies
- skin alterations or states of health that may affect the participation
- participation in other trials if this affects the participation in this trial

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcomes are physiological changes measured via 24-hour ECG, peripheral and central body temperature, respiratory frequency and rhythm before and after the intervention
Secondary Outcome Measures
NameTimeMethod
Further outcomes are subjective sensations measured via psychometric tests and visual analog scales before and after the intervention as well as phenomenological interviews after the intervention
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