Nociceptive Pain Clinical Trial
Official title:
Nociception and BIS Level Monitoring in COVID-19 Patients in the Intensive Care Unit
Pain (nociception), stress and discomfort are difficult to detect in sedated and intubated patients during mechanical ventilation. In order to improve this several nociception level monitors (NOL) were developed that objectively track nociception in sedated or anesthetized patients. Earlier studies showed that for sedated and intubated patients in the operating room, using such monitors is beneficial in reducing stress hormones and post operative pain scores. In this study the investigators aim to observe whether the NOL could be equally beneficial in managing nociception in sedated and intubated ICU patients.
To date it remains challenging to adequately titrate analgesic medication in sedated and anesthetized patients. Recently, nociception monitoring was introduced to guide analgesic treatment in sedated and anesthetized surgical patients. One such monitor is the Nociception Level (NOL; Medasense Biometrics Ltd., Israel). The NOL combines various measurements such as, skin conductance, heart rate, heart rate variability and photoplethysmograph amplitude, and translates these inputs into a single index ranging from 0 (no nociception) to 100 (maximal nociception). Earlier studies have shown that during surgery, the NOL-guided opioid treatment resulted in improved hemodynamics and reduced postoperative pain. In the COVID-19 pandemic, patients admitted in the Intensive Care Unit (ICU), needed excessive amounts of sedatives, analgesics and muscle relaxants during mechanical ventilation. To determine its value in the ICU, the investigators measured NOL values in COVID and non-COVID ICU patients in an earlier study. The aim of the investigators was to verify the assumption that COVID-19 patients were overdosed on opioids. Since the investigators indeed did observe lower NOL values in COVID-19 patients than in non-COVID patients in an earlier study, the investigators expanded the study to determine whether sedatives were equally overdosed, by also measuring the bispectral index (BIS). With this extra information the investigators also hope to determine whether it is feasible to use the NOL in the ICU. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03277872 -
NoL, HR and MABP Responses to Tracheal Intubation Performed With MAC Blade Versus Glidescope
|
N/A | |
Enrolling by invitation |
NCT02485795 -
Observational Study of the Impact of Genetic Testing on Healthcare Decisions and Care in Interventional Pain Management
|
N/A | |
Active, not recruiting |
NCT05732896 -
Comparison of Opioid Consumption During TCI Guided by NOL Index or Standard Care Undergoing Intracranial Tumor Surgery
|
N/A | |
Terminated |
NCT00986258 -
Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Chronic Low Back Pain Taking WHO Step III Analgesics But Showing a Lack of Tolerability
|
Phase 3 | |
Not yet recruiting |
NCT04542798 -
CRF vs WCRF or PRF-DRG in CLBP of FJ Origin and RFA Failure of MBDR: Central Sensitization and Aberrant Nerve Sprouting
|
N/A | |
Recruiting |
NCT05106452 -
Effect of ANI on Intraoperative Opioid Consumption
|
||
Completed |
NCT03303651 -
Monitor-Guided Analgesia During General Anesthesia - Part I
|
N/A | |
Completed |
NCT04137991 -
Nol-Index Guided Remifentanil Analgesia Versus Standard Analgesia During Moderate-to-High Risk Cardiovascular Surgery
|
N/A | |
Recruiting |
NCT05998564 -
Comparison of the Skin Conductance Algesimeter and the Nociception Level Index in the Paediatric Population. An Observational Study.
|
||
Recruiting |
NCT05567822 -
The Impact of Esmolol Administration on Postoperative Recovery
|
N/A | |
Completed |
NCT04567160 -
NOL Index to Compare the Intraoperative Analgesic Effect of Propofol Versus Sevoflurane
|
Phase 4 | |
Completed |
NCT04305015 -
Postoperative Benefits of Intraoperative Nociception Level (NOL) Titration - Pilot
|
N/A | |
Completed |
NCT03761433 -
Intraoperative Nociception and Postoperative Pain
|
||
Completed |
NCT05589935 -
Radicle Relief 1: A Study of Health and Wellness Products on Pain and Other Health Outcomes
|
N/A | |
Completed |
NCT01979718 -
The Post-operative Analgesia of the Virtual Reality Using a Mirror Therapy After Total Knee Arthroplasty
|
N/A | |
Enrolling by invitation |
NCT04435821 -
PET/MRI in the Diagnosis of Pediatric Chronic Pain
|
Phase 1 | |
Completed |
NCT03140241 -
Pain Assessment by Pupil Dilation Reflex (PDR) and Pupillary Pain Index (PPI) in Response to Noxious Stimulation in Anesthetized Adults
|
N/A | |
Completed |
NCT05127200 -
Cervical Neuromodulation and Nociceptive Processing
|
N/A | |
Recruiting |
NCT06313320 -
Intraoperative Electroencephalographic Biomarkers of Postoperative Pain
|
||
Not yet recruiting |
NCT05339737 -
The Nociception Level (NOL) Index for Pain Assessment in the Adult Intensive Care Unit
|