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Pain Measurement and Pain Management in the Intensive Care Unit(ICU)

NCT ID: NCT00773045

Last Updated: 2008-10-16

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

190 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-04-30

Study Completion Date

2007-10-31

Brief Summary

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The purpose of this study is to evaluate the effect of a pain training program and systematic measurement of pain scores on actual pain levels and the use of analgesics in critically ill patients.

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Detailed Description

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Systematic evaluation of pain, though still not common practice in all ICUs, is recommended in clinical practice guidelines for optimal pain management. Pain is a frequently experienced problem in patients in the Intensive Care Unit(ICU). In search of literature to support the need for introduction of a pain management system and to train the entire health staff in our department little information was found concerning the effects of pain training and pain management systems in the ICU. The small number of available studies may be explained by the difficulty of systematic pain measurement in ICU patients, mainly due to the inability to communicate effectively with these patients.

Conditions

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Critically Ill Patients

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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pain training program

ICU Patients treated with or without pain management protocol

A Pain training program and pain measurement

Intervention Type OTHER

Comparing patients treated with and without analgesia and sedation protocol

Interventions

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A Pain training program and pain measurement

Comparing patients treated with and without analgesia and sedation protocol

Intervention Type OTHER

Other Intervention Names

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pain measurement pain management

Eligibility Criteria

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Inclusion Criteria

* All patients admitted to the ICU of the St. Antonius hospital, \>18 years old.

Exclusion Criteria

* Patients who are suspected to be brain-dead
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Antonius Hospital

OTHER

Sponsor Role lead

Responsible Party

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St Antonius Hospital

Principal Investigators

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Peter Bruins, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Anaesthesiology, Intensive Care and Pain Management, St Antonius Hospital, Nieuwegein

Other Identifiers

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PIJNICU2/Z06.11

Identifier Type: -

Identifier Source: org_study_id

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