Actively Recruiting

Age: 18Years +
All Genders
NCT05873894

Acute Pain Oscillation in Electroencephalographic Monitoring Under General Anaesthesia

Led by Hospital General Universitario de Valencia · Updated on 2023-07-24

50

Participants Needed

2

Research Sites

291 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic pain is an undesirable condition that impacts predominantly quality of life at all levels. Chronic pain might occur in healthy young patients when acute postoperative pain is undertreated and persists in time. There are some indexes in the market to evaluate pain, but they assess mainly parasympathetic activity. Hence, it´s a measure of the physiological response to pain, which is still a not well-defined concept. Patients under General Anesthesia might be experimenting unnoticed pain as there is no direct standard method to measure it in clinical practice. This study aims to detect brain oscillatory activity in the intraoperative setting in four situations; awake-no pain, awake-pain, sleep-no pain, and sleep-pain. Pain can be assessed by studying the local and global dynamics of brain activity. A promising upcoming measure of pain could be implemented in clinical practice to detect and treat pain.

CONDITIONS

Official Title

Acute Pain Oscillation in Electroencephalographic Monitoring Under General Anaesthesia

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients that undergo schedule neurosurgery with neurophysiological monitorisation.
  • American Society of Anaesthesiologist physical status (ASA) I-IV.
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Obstructive hydrocephaly with or with a derivative catheter.
  • Patients with neurostimulator
  • Emergency surgery.

AI-Screening

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Trial Site Locations

Total: 2 locations

1

CHGUV

Valencia, Spain, 46014

Actively Recruiting

2

CHGUV

Valencia, Spain

Actively Recruiting

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Research Team

C

Carolina S Romero, PhD

CONTACT

P

Paula Solis, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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