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Fentanyl Ultra Low Doses Effects on the Nociceptive Threshold (FENTANULD)

Primary Purpose

Pain, Postoperative

Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Fentanyl/Placebo injection
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Pain, Postoperative focused on measuring Postoperative Hyperalgesia, Human volunteer, Fentanyl, Randomized Controlled Trial, Pain chronicisation, Predictive test

Eligibility Criteria

18 Years - 40 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

In both groups:

  • 18-40 years old male volunteer
  • Weight: 60 to 85 kg
  • ASA score: 1
  • Informed consent obtained from the patient

In "operated" group:

  • At least one history of peripheral surgery under general anesthesia with opioid in the past five years.

Exclusion Criteria:

In both groups:

  • The patients do not accept inclusion to the study
  • Drug or alcohol abuse history
  • Chronic use of analgesic drugs or history of chronic pain
  • Analgesic or opioid consumption within the 12hs preceding the fentanyl or placebo injection
  • Neurological and/or psychiatric disorder, inability to give informed consent
  • Psychological trauma within the two year preceding the inclusion
  • Any contraindication to fentanyl use
  • Use of any medication interacting with fentanyl
  • Exclusion period from the national healthy volunteer register

In "healthy" group:

  • Any history of general anesthesia or surgery

Sites / Locations

  • CHU de Bordeaux Département d'Anesthésie-Réanimation II

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

1

2

3

4

Arm Description

0,5 µg/kg

0,05 µg/kg

0,005 µg/kg

NaCl 0,9 %

Outcomes

Primary Outcome Measures

Nociceptive threshold evaluated with sternal electronical Von Frey mechanical stimulation. The stimulation will increase until the volunteer presses a trigger when the stimulation becomes painful.

Secondary Outcome Measures

Non invasive blood pressure (SBP, DBP), heart rate, respiratory rate, pulse oxymetry and cognitive functions evaluation (sedation score).

Full Information

First Posted
March 29, 2007
Last Updated
June 2, 2015
Sponsor
University Hospital, Bordeaux
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1. Study Identification

Unique Protocol Identification Number
NCT00454259
Brief Title
Fentanyl Ultra Low Doses Effects on the Nociceptive Threshold
Acronym
FENTANULD
Official Title
Fentanyl Ultra Low Doses Effects on Human Volunteer's Nociceptive Threshold. Towards a Simple Pharmacological Test Able to Predict Pain Vulnerability, Post Operative Hyperalgesia Development Risk?
Study Type
Interventional

2. Study Status

Record Verification Date
March 2007
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
August 2007 (Actual)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital, Bordeaux

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Exaggerated pain and hyperalgesia are major issues after surgery and can lead to chronic pain. Opioid are parts of pain sensitization processes but remain absolutely necessary in the intraoperative period. NMDA receptor antagonists succeed in reducing this pain sensitization process. Recent studies show that in pain and opioid-experienced rats (POER) fentanyl ultra low doses do not induce analgesia, as observed in naive rats, but hyperalgesia. This is the first demonstration that a drug can induce opposite effect depending on individual history. We also observed a strong correlation between this hyperalgesic response in POER and the intensity of hyperalgesia they develop later, after inflammatory or surgical pain. The main aim of this study is to measure the dose effect response to fentanyl "ultra low doses" on human volunteer's nociceptive threshold, to determine if such an opposite response profile can be revealed.
Detailed Description
Principal Objective : "Evaluate fentanyl "ultra low doses" effects on human volunteer's nociceptive threshold depending on their prior pain and opioid experience." Secondary Objective : "Confirm the innocuousness of this test (the 3 "ultra low doses" used in this trial will be 10 to 1,000 fold lower than low doses use for anesthesia and analgesia) and to find the fentanyl ultra low dose that could be used to develop a pain sensitisation predictive test." Study design : Bicentric, prospective, randomized, double-blind study. Inclusion criteria : In both groups: 18-40 years old male volunteer weight: 60 to 85 kg ASA score: 1 Informed consent obtained from the patient Gender : Male In "operated" group: - At least one history of peripheral surgery under general anesthesia with opioid in the past five years Exclusion criteria : In both groups: The patient do not accept inclusion to the study Drug or alcohol abuse history Chronic use of analgesic drugs or history of chronic pain Analgesic or opioid consumption within the 12hs preceding the fentanyl or placebo injection Neurological and/or psychiatric disorder, inability to give informed consent Psychological trauma within the two year preceding the inclusion Any contraindication to fentanyl use Use of any medication interacting with fentanyl Exclusion period from the national healthy volunteer register Gender : Female In "healthy" group: - Any history of general anesthesia or surgery Study plan: comparing two groups that only defer by their surgical and opioid prior experience and will receive three fentanyl ultra low doses (10 to 1,000 fold lower than low doses use for anesthesia and analgesia) and placebo (cross over administration, one week wash out period). Number of subjects : 48

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative
Keywords
Postoperative Hyperalgesia, Human volunteer, Fentanyl, Randomized Controlled Trial, Pain chronicisation, Predictive test

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
0,5 µg/kg
Arm Title
2
Arm Type
Experimental
Arm Description
0,05 µg/kg
Arm Title
3
Arm Type
Experimental
Arm Description
0,005 µg/kg
Arm Title
4
Arm Type
Placebo Comparator
Arm Description
NaCl 0,9 %
Intervention Type
Drug
Intervention Name(s)
Fentanyl/Placebo injection
Intervention Description
Ultra low dose intravenous injection
Primary Outcome Measure Information:
Title
Nociceptive threshold evaluated with sternal electronical Von Frey mechanical stimulation. The stimulation will increase until the volunteer presses a trigger when the stimulation becomes painful.
Time Frame
5 min after injection, and every 15 min during 1 hour
Secondary Outcome Measure Information:
Title
Non invasive blood pressure (SBP, DBP), heart rate, respiratory rate, pulse oxymetry and cognitive functions evaluation (sedation score).
Time Frame
all along the experimentation

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: In both groups: 18-40 years old male volunteer Weight: 60 to 85 kg ASA score: 1 Informed consent obtained from the patient In "operated" group: At least one history of peripheral surgery under general anesthesia with opioid in the past five years. Exclusion Criteria: In both groups: The patients do not accept inclusion to the study Drug or alcohol abuse history Chronic use of analgesic drugs or history of chronic pain Analgesic or opioid consumption within the 12hs preceding the fentanyl or placebo injection Neurological and/or psychiatric disorder, inability to give informed consent Psychological trauma within the two year preceding the inclusion Any contraindication to fentanyl use Use of any medication interacting with fentanyl Exclusion period from the national healthy volunteer register In "healthy" group: Any history of general anesthesia or surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe RICHEBE, Dr
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Gérard JANVIER, PHD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claude DUBRAY, PHD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alain ESCHALIER, PHD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
jean DUALE CHRISTIAN, Dr
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gisèle PICKERING, Dr
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Bordeaux Département d'Anesthésie-Réanimation II
City
PESSAC Cedex
State/Province
Hôpital cardiologique
ZIP/Postal Code
33604
Country
France

12. IPD Sharing Statement

Citations:
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16129988
Citation
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PubMed Identifier
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Citation
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Citation
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Citation
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Citation
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Citation
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Results Reference
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Fentanyl Ultra Low Doses Effects on the Nociceptive Threshold

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