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Exploratory study of proof of concept of safety and comfort efficacy of a pneumatic knee massager.

Exploratory study of proof of concept of safety and comfort efficacy of a pneumatic knee massager. - pneuMO1

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00024114
Enrollment
30
Registered
2021-01-19
Start date
2020-11-01
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

healthy volunteer

Interventions

Group 1: 30 min Applikation of Pneumatic Knee Massagen resting postition

Sponsors

Institut Prof. Kurscheid
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Willingness to participate in the study (signed consent form) Age: older than 18 years

Exclusion criteria

Exclusion criteria: Subjects with open wounds or wound sutures in the application area Subjects with arthroscopy in the last 6 months

Design outcomes

Primary

MeasureTime frame
Relative number of subjects who reported positive wearing comfort or added value after 30 min application

Secondary

MeasureTime frame
Number of reported functional disturbances during application Intraindividual change in knee circumference before and after application. Intraindividual difference in change before and after application of knee circumference between right and left knee. Relative number of subjects who experienced a side effect (pain or tenderness or other side effects) in at least one application. after 30 min application

Countries

Germany

Contacts

Public ContactThomas Kurscheid

Institut Prof. Kurscheid

info@dr-kurscheid.de0221 8004320

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026