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Modulation of Remifentanil-induced Postinfusion Hyperalgesia

Primary Purpose

Hyperalgesia, Secondary

Status
Completed
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
Placebo
Remifentanil
Ketorolac and remifentanil
Parecoxib and remifentanil
Sponsored by
Ullevaal University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Hyperalgesia, Secondary focused on measuring hyperalgesia, remifentanil, ketorolac, parecoxib, COX-1 inhibitor, COX-2 inhibitor

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy volunteers

Exclusion Criteria:

  • Allergy to the drugs used in the study

Sites / Locations

  • Ullevaal University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Placebo

Remifentanil

Ketorolac and remifentanil

Parecoxib and remifentanil

Arm Description

Outcomes

Primary Outcome Measures

H0 : Parecoxib prevents remifentanil postinfusion secondary hyperalgesi. Ketorolac does not prevent remifentanil postinfusion secondary hyperalgesi.

Secondary Outcome Measures

HA : Parecoxib and ketorolac prevent remifentanil postinfusion secondary hyperalgesi.

Full Information

First Posted
November 4, 2008
Last Updated
June 30, 2011
Sponsor
Ullevaal University Hospital
Collaborators
University of Oslo, Rikshospitalet University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00785863
Brief Title
Modulation of Remifentanil-induced Postinfusion Hyperalgesia
Official Title
Modulation of Remifentanil-induced Analgesia and Postinfusion Hyperalgesia by Parecoxib or Ketorolac in Humans
Study Type
Interventional

2. Study Status

Record Verification Date
November 2008
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Ullevaal University Hospital
Collaborators
University of Oslo, Rikshospitalet University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In addition to alleviate pain there is growing evidence that µ-opioids enhance pain. This problem is known as opioid induced hyperalgesia(OIH).The NMDA receptor is involved in opioid induced hyperalgesia it may be possible to block OIH by cyclooxygenase inhibitors. This has been demonstrated with parecoxib, a COX-II inhibitor, in a experimental pain model.Both COX-1 and COX-2 are expressed in the spinal cord. It would be of interest to investigate whether a COX-1 preferring inhibitor like ketorolac also can reduce opioid induced hyperalgesic in this experimental pain model.
Detailed Description
Remifentanil is an fast acting opioid which has become very popular to use during surgery. There are studies, both experimental 1-3 and clinical 4;5, which indicate that remifentanil after end of infusion trigger enhanced pain experience and enhanced opioid consumption postoperatively. Therefore it is important to look at possibilities to block this enhanced pain experience (opioid induced hyperalgesia - OIH). Ketamin has demonstrated to block this effect 5;6 through the NMDA receptor. Unfortunately ketamin has some seriously side-effects like hallucinations, and is therefore not suitable in ordenary clinical use. Recently, it has been demonstrated that parecoxib (a COX-2 inhibitor) can prevent remifentanil-induced postinfusion hyperalgesia in a study on healthy volunteers.7 COX-2 inhibitors have some disadvantages because of the longterm adverse effects like cardiac arrest. Therefore it would be of interest to look at a COX-1 preferring NSAID, like ketorolac, to see if also non-selective NSAIDs can partly block remifentanil-induced postinfusion hyperalgesia. To investigate this and to provoke pain and secondary hyperalgesia we use an intradermal electrical pain model which is well established.1;7-9 Detailed description of this model look at reference 7. H0 : Parecoxib prevents remifentanil postinfusion secondary hyperalgesi. Ketorolac does not prevent remifentanil postinfusion secondary hyperalgesi HA : Parecoxib and ketorolac prevent remifentanil postinfusion secondary hyperalgesi.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperalgesia, Secondary
Keywords
hyperalgesia, remifentanil, ketorolac, parecoxib, COX-1 inhibitor, COX-2 inhibitor

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Remifentanil
Arm Type
Active Comparator
Arm Title
Ketorolac and remifentanil
Arm Type
Active Comparator
Arm Title
Parecoxib and remifentanil
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo IV before placebo infusion
Intervention Type
Drug
Intervention Name(s)
Remifentanil
Other Intervention Name(s)
Ultiva
Intervention Description
placebo IV and remifentanil infusion
Intervention Type
Drug
Intervention Name(s)
Ketorolac and remifentanil
Other Intervention Name(s)
Toradol
Intervention Description
Ketorolac IV and remifentanil infusion
Intervention Type
Drug
Intervention Name(s)
Parecoxib and remifentanil
Other Intervention Name(s)
Dynastat
Intervention Description
Parecoxib IV and remifentanil infusion
Primary Outcome Measure Information:
Title
H0 : Parecoxib prevents remifentanil postinfusion secondary hyperalgesi. Ketorolac does not prevent remifentanil postinfusion secondary hyperalgesi.
Time Frame
during the study
Secondary Outcome Measure Information:
Title
HA : Parecoxib and ketorolac prevent remifentanil postinfusion secondary hyperalgesi.
Time Frame
During the study

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy volunteers Exclusion Criteria: Allergy to the drugs used in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harald Lenz, MD
Organizational Affiliation
Ullevaal University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Johan Raeder, Prof.,MD,PhD
Organizational Affiliation
Ullevaal University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Audun Stubhaug, Prof.,MD,PhD
Organizational Affiliation
Rikshospitalet University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Ullevaal University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway

12. IPD Sharing Statement

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Modulation of Remifentanil-induced Postinfusion Hyperalgesia

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