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Blood volume changes in skeletal muscle.

Blood volume changes in skeletal muscle measured with power Doppler ultrasound during whole body exercise: reproducability and validity.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24988
Enrollment
30
Registered
2015-11-16
Start date
2015-12-06
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

vascular endothelium dysfunction, dysfunction arteries, skeletal muscle, blood volume changes.

Interventions

The study is designed as a prospective observational study without invasive measurements on healthy subjects. After informed consent is obtained a baseline assessment will be performed. This assessmen

Sponsors

Máxima Medisch Centrum
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Written informed consent Age 18-50 years. Able to perform a maximal exercise test.

Exclusion criteria

Exclusion criteria: Subjects with risk of adverse events according to abnormal findings in physical examination or the Lausanne questionnaire. Orthopaedic,cardio-vascular, pulmonary, neuromuscular and other diseases limiting exercise capacity.

Design outcomes

Primary

MeasureTime frame
Reproducibility: Difference and agreement (bias and limits of agreement) of changes in blood volume assessed by power Doppler in the vastus lateralis muscle during maximal and submaximal exercise on two separate days.

Secondary

MeasureTime frame
Validity: - Correlation between changes in power Doppler-signal in the musculus vastus lateralis and changes in blood flow in the afferent artery measured with pulsed wave Doppler during exercise. - Correlation between changes in total hemoglobulin measured with near infrared spectroscopy and changes in Power Doppler-signal during exercise.

Contacts

Public ContactThijs Schoots

Máxima Medisch Centrum (department Cardiology)

thijs.schoots@mmc.nltel.: 040-8888200

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)