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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03016221
Other study ID # 2016-01541
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2017
Est. completion date December 6, 2019

Study information

Verified date June 2019
Source University of Applied Sciences and Arts of Southern Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The use of topical over-the-counter (OTC) products with a warming or cooling effect is widespread in the fields of sport, physiotherapy and in private households. Advertisements for such products promise pain relief when suffering from musculoskeletal disorders such as muscle tension, rheumatism or acute injuries, e.g. sprains. In literature, there are only little information about the efficacy and the physiological mechanisms of topical warming or cooling products. Therefore, the aim of this study is to investigate the local skin characteristics during and after an application of a topical product with a warming or cooling effect.


Description:

The use of topical products for local pain relief in chronic or acute musculoskeletal disorders is widely used. Despite the widespread use of these products, there is missing information on the physiological mechanisms and efficacy of topical warming and cooling ointments. Most of the existing literature is about the efficacy of topical non-steroidal anti-inflammatory drug (NSAID)-products on chronic pain in osteoarthritis. Furthermore, one study tested the cooling effect of gels with different menthol concentrations. They found that, regardless of the concentration, the skin temperature was reduced up to one hour post application in the area of application.

The aim of our study is to evaluate the change of skin characteristics after a single application of a warming or cooling topical product on healthy subjects. Outcome parameters include skin perfusion, temperature, skin redness and subjective thermal sensation. We only selected products in form of alcohol based ointments, menthol or wintergreen oil. Sprays and patches were excluded.

The application area is the unilateral lumbar back region, whereas the contralateral side serves as control area. After an acclimatization period, baseline measurements are performed, followed by standardized application of the topical product. The local skin responses are measured in 10 mins time increments up to one hour.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date December 6, 2019
Est. primary completion date December 6, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- no existing musculoskeletal disorders in the region of interest

- no surgery in the region of interest in the last year

- healthy skin conditions in the region of interest

Exclusion Criteria:

- fear of treatment

- regular intake of drugs, excluding contraceptives

- metal implants in the region between C7 and sacrum, including hip joints

- lack of epicritic and protopathic skin sensitivity

- renal insufficiency

- bronchial asthma

- pregnancy/lactation

- type 1 or 2 diabetes mellitus

- polyneuropathy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Axanova hot gel
Axanova hot gel is a topical product with a warming effect. It contains menthol, pine needle oil, wintergreen oil, rosemary oil, eucalyptus oil, incense oil.
Axanova activ gel
Axanova activ gel is a topical product with a revulsive effect. It contains menthol, pine needle oil, orange oil, lemon oil, wintergreen oil, glycosaminoglycans.
Perskindol Dolo Gel
Perskindol Dolo Gel is a topical product with a warming effect. It contains wintergreen oil, pine needle oil, aromatics, excipients.
Perskindol Classic Gel
Perskindol Classic Gel is a topical product with a revulsive effect. It contains menthol, wintergreen oil, pine needle oil, lemon oil, orange peel oil, lemon bergamot oil, rosemary oil, lavender oil, excipients.
Perskindol Cool Kühl-Gel
Perskindol Cool Kühl-Gel is a topical product with a cooling effect. It contains levomenthol, color E131, aromatics, excipients.
Dolor-X Hot Gel
Dolor-X Hot Gel is a topical product with a warming effect. It contains isopropyl alcohol, water, menthol, hyprolose, camphor, trometamol, paprika, wintergreen oil, excipients.
Dolor-X Classic Gel
Dolor-X Classic Gel is a revulsive product. It contains water, isopropyl alcohol, menthol, spruce, hyprolose, trometamol, wintergreen oil, excipients.
Dolor-X Cool Gel
Dolor-X Cool Gel is a cooling product. It contains water, isopropyl alcohol, menthol, trometamol, color E131, excipients.

Locations

Country Name City State
Switzerland SUPSI Landquart GR

Sponsors (1)

Lead Sponsor Collaborator
University of Applied Sciences and Arts of Southern Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary local skin perfusion local skin perfusion will be measured with a laser speckle instrument during one hour post application
Primary local skin redness local skin redness (erythema) will be measured with a chromameter during one hour post application
Primary skin surface temperature skin surface temperature will be measured with thermochrons, infrared thermometer and thermal imaging camera during one hour post application
Primary local muscle tissue oxygenation local muscle tissue oxygenation will be measured with near infrared spectroscopy during one hour post application
Primary subjective temperature sensation subjective temperature sensation will be evaluated with a thermal comfort questionnaire during one hour post application
Secondary skin perfusion directly next to the application area skin perfusion will be measured with a laser speckle instrument during one hour post application
Secondary skin redness directly next to the application area skin redness (erythema) will be measured with a chromameter during one hour post application
Secondary skin temperature directly next to the application area skin surface temperature will be measured with thermochrons, infrared thermometer and thermal imaging camera during one hour post application
Secondary muscle tissue oxygenation directly next to the application area muscle tissue oxygenation will be measured with near infrared spectroscopy during one hour post application
Secondary subjective temperature sensation directly next to the application area subjective temperature sensation will be evaluated with a thermal comfort questionnaire during one hour post application
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