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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05873894
Other study ID # 31/2020
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 15, 2023
Est. completion date December 15, 2028

Study information

Verified date July 2023
Source Hospital General Universitario de Valencia
Contact Carolina S Romero, PhD
Phone +34963187554
Email romero_carolinasol@gva.es
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

This is a pilot study of the presence of neural oscillations during acute pain while awake and in the anesthetized patient with neurophysiological monitoring during a neurosurgery surgical intervention analyzed by electroencephalography. After the patient's consent, the electroencephalogram is placed in the awake patient and a small painful stimulus is performed based on the channeling of a second venous access. In turn, a recording of the EEG waves is made in order to identify similar neuronal waves during the surgical procedure once the patient is under general anesthesia. The reason for this intervention is to have a baseline record of each patient without interfering with the oscillations of the different drugs used during total intravenous anesthesia used in these procedures. Normally, after general anesthesia, between 3 and 6 electrodes would be placed on the scalp and 10 electrodes would be placed to carry out this work. After the intervention, a telephone survey will be carried out on postoperative pain at 3 months and a year.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 15, 2028
Est. primary completion date December 15, 2027
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients that undergo schedule neurosurgery with neurophysiological monitorisation. - American Society of Anaesthesiologist physical status (ASA) I-IV. Exclusion Criteria: - Pregnancy - Obstructive hydrocephaly with or with a derivative catheter. - Patients with neurostimulator - Emergency surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
EEG
EEG recordings and analysis. Sensory evoked potentials analysis Motor evoked potentials studies

Locations

Country Name City State
Spain CHGUV Valencia
Spain CHGUV Valencia

Sponsors (1)

Lead Sponsor Collaborator
Hospital General Universitario de Valencia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oscillations related to pain in the EEG The main objective is the characterization and evaluation of the neural oscillations in the EEG that occur in the anesthetized patient when acute intraoperative pain occurs during monitoring by neurophysiology in neurosurgery.
The current procedure includes patient monitoring with neurophysiology electrodes at muscle level and EEG for proper mapping of the functions to be explored when the patient is under the effects of general anesthesia.
To carry out this work, it would be necessary to monitor the EEG with the patient awake, since it is intended to look for the characteristic neural oscillations at the moment in which the second peripheral venous line is cannulated.
since start of surgery until the end
Secondary Incidence of Chronic pain Develop an objective scale of pain in the patient under general anesthesia.
Evaluate the degree of pain 3 months after surgery using the visual analogue scale in the operated patients or/and Pain Detect Questionnarie .
after surgery until 1 year post surgery
Secondary opiod consumption During the intraoperative phase we will base ourselves on the equivalence between the use of intravenous fentanyl or oxycodone and intravenous morphine. For the subsequent evaluation of opioid consumption one year after surgery, we will base ourselves on the conversion tables to oral morphine. during surgery until 1 year post surgery
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