MSOT beeldvorming in de onderbenen van gezonde vrijwilligers.

• Conditions: peripheral atheroslerosis.

• Registration Number: NL-OMON27078
• Lead Sponsor: niversity Medical Center Groningen

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 10

Inclusion Criteria

Ten (10) healthy volunteers (5 males and 5 females), age >18 years will be asked to participate.

-No prior or current medication.

Exclusion Criteria

-Medical or psychiatric conditions that compromise the volunteers' ability to give informed consent.

-Concurrent uncontrolled medical conditions.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary endpoints are to determine measurement variation (mean and SD) of MSOT in physiological perfused lower leg.

Secondary Outcome Measures

Name	Time	Method
Information on safety aspects of the MSOT imaging device, side effects, adverse events (AE), serious adverse events (SAE) and suspected unexpected serious adverse reactions (SUSAR).