Application of the ELFI-TECH monitor for measurement of nociceptio

Completed

• Conditions: monitoring; hemodynamics; pain measurements

• Registration Number: NL-OMON42818
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

Subjects of either sex, aged 18-34 years with a body mass index < 30 kg/m2.

Exclusion Criteria

Severe medical disease including hypertension, liver/renal disease, neurological disorders, diaphragmatic hernia/pyrosis; (history of) psychiatric or neurological disease; pregnancy/lactation; allergy to study medication; (history of) illicit drug abuse/alcoholism.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Elfitor</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Cardiac output<br /><br>Blood pressure<br /><br>Pulse oximetry<br /><br>ECG monitoring<br /><br>NoL</p><br>