Pupillometry for Pain Assessment in Critically Ill Patients
NCT ID: NCT02576132
Last Updated: 2015-10-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
80 participants
OBSERVATIONAL
2011-11-30
2012-10-31
Brief Summary
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Being in pain is reported to be one of the most important stressors in critically ill patients and worsens outcome. The evaluation of pain using validated scores in patients who are able to self-report significantly improves the quality of analgesic therapy and health related outcomes in intensive care patients.
However, behavioral pain score that are used in sedated or delirious patients, often underestimate the severity of pain.
The primary aim of this study is to investigate if measurement of the pupillary light reflex Amplitude correlates with the results of pain assessment using validated pain scores in critically ill patients.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* aged 18 years or older
* patients with an expected intensive care unit length of stay of of at least 48 hours.
Exclusion Criteria
* traumatic brain injury
* stroke
* increased intracranial pressure
* ocular disease or surgery.
18 Years
ALL
No
Sponsors
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Charite University, Berlin, Germany
OTHER
Responsible Party
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Claudia Spies
Head of Department of Anesthesiology and Intensive Care Medicine CVK/CCM
Principal Investigators
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Claudia Spies, MD Prof.
Role: STUDY_DIRECTOR
Charité - Univeritätsmedizin Berlin
Locations
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Department of Anesthesiology and Intensive Care Medicine CVK/CCM, Charité - University Medicine
Berlin, State of Berlin, Germany
Countries
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Other Identifiers
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Vola-ICU
Identifier Type: -
Identifier Source: org_study_id
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