Validation of CPM#1 compressibility in healthy volunteers in rest and after exercise

Validation of CPM#1 compressibility in healthy volunteers in rest and after exercise - Non-invasive measurement of compartment pressure: Reliability

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON56011

Enrollment

Registered

2022-11-29

Start date

2023-02-02

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Chronic Exertional Compartment Syndrom Lower Leg Pain

Interventions

None listed

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - >= 18 years - Proficient in speaking and reading Dutch

Exclusion criteria

Exclusion criteria: - Presence or history of CECS - History of surgery or other trauma which penetrated the fascia of the leg - Other concurrent limb pathologies or anomalies amongst others: - Peripheral arterial or venous disease - Muscle disorders, diabetes mellitus, peripheral neuropathies - Unable to exercise for 5-minutes - Open wound at site of measurement

Design outcomes

Primary

Measure	Time frame
Inter-observer reliability of the compressibility measured with CPM#1 device	—

Secondary

Measure	Time frame
- To clinically validate the intra-observer reliability of compressibility measurements with the CPM#1 device during rest in healthy volunteers. - To investigate the effect of exercise on compressibility immediately, one minute, and five minutes after exercise in healthy volunteers.	—

Countries

Netherlands

Outcome results