search
Back to results

Pupillometry and Nociception Level Index for the Evaluation of Pain in Intensive Care Unit. (NOCI-ICU)

Primary Purpose

Critical Illness

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Systemic pain assessment
Sponsored by
Centre Hospitalier Régional d'Orléans
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Critical Illness focused on measuring pain, intensive care, sedated, ventilated, NOL ICU, pupillometry

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • older than18 years old
  • Under invasive mechanical ventilation
  • Sedated with i) a Richmond Agitation Sedation Scale (RASS) : ≥ -4 and <1, ii) being unable to evaluate their pain by a visual numeric scale

Exclusion Criteria:

  • Ophthalmological diseases which could modify the pupillometric parameters
  • Neurological diseases (damage of nerve III, intracranial hypertension, stroke)
  • Admitted in ICU after resuscitated cardiac arrest
  • Drugs that inhibit the effect of the sympathetic system (clonidine, dexmedetomidine)
  • Patient under Veno-Arterial Extracorporeal Membrane Oxygenation (VA-ECMO)
  • Patient treated by a neuromuscular blockade
  • A do-not resuscitate order
  • Major hemodynamic instability prohibiting planned care procedures

Sites / Locations

  • Regional Hospital Center
  • Universitary Hospital Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Pupillometry

Arm Description

Pain will be evaluated via pupillometry with 3 successive measurements

Outcomes

Primary Outcome Measures

pupillary redilatation velocity after constriction light-induced
Area under the ROC curve (AUC) of pupillary re-dilation velocity measured before a potentially painful procedure to predict the occurrence of a BPS score ≥ 5 during the procedure.

Secondary Outcome Measures

Nociception Level index
To evaluate the predictive value of the NOL-index measured before a potentially painful procedure to predict the intensity of the pain felt during the procedure.
Systolic and diastolic Blood pressure
Describe the variations of vital parameters
Heart rate
Describe the variations of vital parameters
Respiratory rate
Describe the variations of vital parameters
Behaviour Pain Scale
Compare variations of nociception parameters during mobilizations and during tracheal aspirations Behaviour Pain Scale Score from 3 (no pain) to 12 (maximum pain)

Full Information

First Posted
June 20, 2022
Last Updated
March 31, 2023
Sponsor
Centre Hospitalier Régional d'Orléans
search

1. Study Identification

Unique Protocol Identification Number
NCT05469841
Brief Title
Pupillometry and Nociception Level Index for the Evaluation of Pain in Intensive Care Unit.
Acronym
NOCI-ICU
Official Title
Pupillometry and Nociception Level Index (NOL-index) for the Evaluation of Pain in Intensive Care Unit. Prospective Study in Two Centers
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
July 29, 2022 (Actual)
Primary Completion Date
March 28, 2023 (Actual)
Study Completion Date
March 28, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Régional d'Orléans

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Pain is a frequent symptom in the intensive care unit (ICU). Critical ill patients are often intubated and sedated which makes self-evaluation of pain impossible. Pupillary dilatation is a reflex directly related to stimuli such as pain, which can be measured by quantitative pupillometry. Several studies in ICU showed a significant relationship between pupillary diameter variation and pain. The nociception level index (NOL-index) is a recent noninvasive and continuous monitoring of pain essentially used in operating room. The aim of this study is to evaluate the pupillometry and NOL index in critical ill patients in sedated patients under mechanical ventilation during the mobilization plus toilet (described in literature as not painful procedure) and tracheal suctioning (described as a painful procedure)
Detailed Description
Pain will be evaluated via i) pupillometry with 3 successive measurements ii) Behaviour Pain Scale (BPS) and Critical Care Pain Observation Tool (CPOT) score evaluated by an investigator (physician) iii) evolution of physiological parameters (ie heart rate, blood pressure, respiratory rate) iv) Nociception level index (NOL-index). The evaluation times will be 5 minutes before care procedures (mobilization plus toilet and tracheal suctioning), during the procedures (with the worst value recorded) and 5 minutes after the procedures. The procedures are: A mobilization and toilet of the patient: a priori, not a very painful procedure. The pain will be evaluated every 5 minutes during the toilet. Tracheal suctioning: a procedure known to be painful. The painful will be evaluated just at the end of tracheal suctioning (once the tracheal suctioning catheter is removed from the endotracheal intubation).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness
Keywords
pain, intensive care, sedated, ventilated, NOL ICU, pupillometry

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pupillometry
Arm Type
Experimental
Arm Description
Pain will be evaluated via pupillometry with 3 successive measurements
Intervention Type
Other
Intervention Name(s)
Systemic pain assessment
Intervention Description
Pain will be evaluated via i) pupillometry with 3 successive measurements ii) Behaviour Pain Scale (BPS) and Critical Care Pain Observation Tool (CPOT) score evaluated by an investigator (physician) iii) evolution of physiological parameters (ie heart rate, blood pressure, respiratory rate) iv) Nociception Level Index (NOL) index.
Primary Outcome Measure Information:
Title
pupillary redilatation velocity after constriction light-induced
Description
Area under the ROC curve (AUC) of pupillary re-dilation velocity measured before a potentially painful procedure to predict the occurrence of a BPS score ≥ 5 during the procedure.
Time Frame
1 hour during procedure
Secondary Outcome Measure Information:
Title
Nociception Level index
Description
To evaluate the predictive value of the NOL-index measured before a potentially painful procedure to predict the intensity of the pain felt during the procedure.
Time Frame
1 hour during procedure
Title
Systolic and diastolic Blood pressure
Description
Describe the variations of vital parameters
Time Frame
1 hour during procedure
Title
Heart rate
Description
Describe the variations of vital parameters
Time Frame
1 hour during procedure
Title
Respiratory rate
Description
Describe the variations of vital parameters
Time Frame
1 hour during procedure
Title
Behaviour Pain Scale
Description
Compare variations of nociception parameters during mobilizations and during tracheal aspirations Behaviour Pain Scale Score from 3 (no pain) to 12 (maximum pain)
Time Frame
1 hour during procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: older than18 years old Under invasive mechanical ventilation Sedated with i) a Richmond Agitation Sedation Scale (RASS) : ≥ -4 and <1, ii) being unable to evaluate their pain by a visual numeric scale Exclusion Criteria: Ophthalmological diseases which could modify the pupillometric parameters Neurological diseases (damage of nerve III, intracranial hypertension, stroke) Admitted in ICU after resuscitated cardiac arrest Drugs that inhibit the effect of the sympathetic system (clonidine, dexmedetomidine) Patient under Veno-Arterial Extracorporeal Membrane Oxygenation (VA-ECMO) Patient treated by a neuromuscular blockade A do-not resuscitate order Major hemodynamic instability prohibiting planned care procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mai Anh NAY, MD
Organizational Affiliation
Regional Hospital Center of ORLEANS
Official's Role
Study Director
Facility Information:
Facility Name
Regional Hospital Center
City
Orléans
ZIP/Postal Code
45067
Country
France
Facility Name
Universitary Hospital Center
City
Tours
ZIP/Postal Code
37000
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Pupillometry and Nociception Level Index for the Evaluation of Pain in Intensive Care Unit.

We'll reach out to this number within 24 hrs