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Co-analgesic Effects of Dexamethasone and Pregabalin After Lumbar Slipped Disc Surgery (DEXA-PG-HD)

Primary Purpose

Patients Undergoing a Lumbar Slipped Disc Surgery

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Pregabaline (150mg), Dexamethasone (20mg/5ml; 0.2mg/kg)
Sponsored by
University Hospital, Clermont-Ferrand
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Patients Undergoing a Lumbar Slipped Disc Surgery focused on measuring Co-analgesia, Dexamethasone, Pregabalin, Lumbar slipped disc surgery, Post-operative pain

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing a lumbar slipped disc surgery
  • Aged 18 to 85 years.
  • ASA score I-III
  • Having given their consent.
  • Affiliated with a social security scheme

Exclusion Criteria:

  • Patients who must be operated urgently.
  • Patients previously operated for lumbar spinal surgery.
  • Expected duration of surgery more than 3 hours.
  • Severe renal impairment defined by a creatinine clearance less than or equal to 30 mL/min.
  • Taking long-term strong opiates .
  • Taking long-term corticosteroids or within 48 hours before surgery.
  • Taking pregabalin or gabapentin within 48 hours before surgery.
  • Drug addiction.
  • Patients with cognitive impairment (judged by the investigator) that may interfere with:

informed consent, the collection of endpoints, the use of auto-controlled analgesia.

  • Pregnant or nursing women.
  • Refusal of the protocol.
  • Minor or major protected patients.
  • Allergy or other cons-indication to the molecules used in the protocol.

Sites / Locations

  • CHU Clermont-Ferrand

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Pregabaline (150mg), Dexamethasone (20mg/5ml; 0.2mg/kg)

Lactose (150mg), NaC1 0.9% (50ml)

Arm Description

The aim of the study is to show a decrease in postoperative pain during the first postoperative mobilization surgery lumbar disc herniation through a co-analgesia with a single dose of dexamethasone, pregabalin, or a combination of these two products

The aim of the study is to show a decrease in postoperative pain during the first postoperative mobilization surgery lumbar disc herniation through a co-analgesia with a single dose of dexamethasone, pregabalin, or a combination of these two products

Outcomes

Primary Outcome Measures

Pain
Pain evaluated by ENS during the first mobilization at the edge of the bed

Secondary Outcome Measures

Pain
Quality of the standing up (evaluated by Likert scale)
Patient satisfaction (evaluated by Likert scale)
Consumption of morphine
Pain at rest
assessment of neuropathic component DN4 scale
statement of analgesic treatment
Pain during mobilization
Postoperative Nausea and Vomiting
Postoperative Nausea and Vomiting
Sedation
Sedation
Sedation
Sedation
Existence of visual disturbances
Existence of lightheadedness
Existence of urinary retention
Existence of pruritus
Pain
pain
pain
pain
pain
pain
pain
pain

Full Information

First Posted
December 4, 2012
Last Updated
May 23, 2019
Sponsor
University Hospital, Clermont-Ferrand
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1. Study Identification

Unique Protocol Identification Number
NCT01811251
Brief Title
Co-analgesic Effects of Dexamethasone and Pregabalin After Lumbar Slipped Disc Surgery
Acronym
DEXA-PG-HD
Official Title
Co-analgesic Effects of Dexamethasone and Pregabalin After Lumbar Slipped Disc Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
December 2012 (Actual)
Primary Completion Date
September 19, 2017 (Actual)
Study Completion Date
October 10, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Clermont-Ferrand

4. Oversight

5. Study Description

Brief Summary
The aim of the study is to show a decrease in postoperative pain during the first postoperative mobilization surgery lumbar disc herniation through a co-analgesia with a single dose of dexamethasone, pregabalin, or a combination of these two products. Pain assessed by simple numerical scale will be also evaluated during the 48 first post-operative hours. Determining an optimal co-analgesic protocol through the results of this study could help develop validation studies with larger scale such as a medico-economic component. In addition, these study protocols are easy to apply (ponctual administration) and inexpensive.
Detailed Description
Visit 1 (J-30 J-1): pre-inclusion visit During a follow-up visit usual pathology, the doctor will propose to the patient to participate in the protocol. Information Form will be given to the patient to be read at home to maintain a sufficient time for reflection. Physician investigator check the eligibility criteria and complete a pre-screening form where he will note the following information about the patient: No pre-enrollment, name, date, reason for non-inclusion appropriate. Visit 2 (J-1): pre-anesthetic visit, the day before surgery During the pre-anesthetic routine consultation, the doctor will check the proper collection of informed consent and then inform the following information on the CRF: randomization number, age, height, weight, ideal weight theory, gender patient. Visit 3 (J0): surgery One hour before surgery, the patient will receive, according to randomization, premedication with pregabalin LYRICA ® or placebo orally. Then the patient will be conducted in the operating room for induction of general anesthesia and surgery. Immediately after induction of anesthesia, depending on randomization, the patient will receive intravenous dexamethasone or placebo. At the end of surgery, the patient is conducted in Post Anaesthesia Carry Unit (PACU) to be extubated and receive routine care after surgery. Extubation of the patient, denoted H0 represents the time when the measurement begins. The data collected from H0 are : ENS score standing at H0, H0+30mn, H0+1h, H0+1h30, H0+2 h, H0+6 h,H0+12 h, H0+24h, H0+48 h. ENS score mobilization at the first time the patient gets up (edge of the bed and standing if possible) Qualification of the quality of standing 0-4 (Likert scale (0 = very poor, 1 = poor, 2 = fair, 3 = good, 4 = very good)) by the nursing staff after the first mobilization Qualification of patient satisfaction compared to the first standing by a score of 0-4 (Likert scale (0 = very poor, 1 = poor, 2 = fair, 3 = good, 4 = very good)) Sedation score at the end of SSPI, , at H0+24h and H0+48h Nausea and vomiting score at H0+24 h, H0+48 h Tolerance of the treatments undertaken : visual disturbances, lightheadedness, urinary retention, pruritus, measured at the end of SSPI at H0+24 h and H0+48 h Consumption of morphine at H0+24 h and H0+48 h Assessment of pain score at 6 months by score ENS at rest , assessment of neuropathic component by DN4 scale. Statement consumption of analgesic treatments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patients Undergoing a Lumbar Slipped Disc Surgery
Keywords
Co-analgesia, Dexamethasone, Pregabalin, Lumbar slipped disc surgery, Post-operative pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
162 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pregabaline (150mg), Dexamethasone (20mg/5ml; 0.2mg/kg)
Arm Type
Experimental
Arm Description
The aim of the study is to show a decrease in postoperative pain during the first postoperative mobilization surgery lumbar disc herniation through a co-analgesia with a single dose of dexamethasone, pregabalin, or a combination of these two products
Arm Title
Lactose (150mg), NaC1 0.9% (50ml)
Arm Type
Placebo Comparator
Arm Description
The aim of the study is to show a decrease in postoperative pain during the first postoperative mobilization surgery lumbar disc herniation through a co-analgesia with a single dose of dexamethasone, pregabalin, or a combination of these two products
Intervention Type
Drug
Intervention Name(s)
Pregabaline (150mg), Dexamethasone (20mg/5ml; 0.2mg/kg)
Primary Outcome Measure Information:
Title
Pain
Time Frame
at H0+2H, at H0+6h, at H0+12h, at H0+24h, at H0+48h
Title
Pain evaluated by ENS during the first mobilization at the edge of the bed
Time Frame
at J0+1 day
Secondary Outcome Measure Information:
Title
Pain
Time Frame
during the first mobilization with standing up at J1
Title
Quality of the standing up (evaluated by Likert scale)
Time Frame
at J0+1day
Title
Patient satisfaction (evaluated by Likert scale)
Time Frame
at J0+1 day
Title
Consumption of morphine
Time Frame
between H0+2h and H0+24h
Title
Pain at rest
Time Frame
at J0+180 days
Title
assessment of neuropathic component DN4 scale
Time Frame
at J0+180 days
Title
statement of analgesic treatment
Time Frame
at J0+180 days
Title
Pain during mobilization
Time Frame
at J0+180 days
Title
Postoperative Nausea and Vomiting
Time Frame
at H0+24h
Title
Postoperative Nausea and Vomiting
Time Frame
at H0+48h
Title
Sedation
Time Frame
at J0 at the arrival in the operating room
Title
Sedation
Time Frame
at J0 at the end of SSPI
Title
Sedation
Time Frame
at H0+24 h
Title
Sedation
Time Frame
at H0+48h
Title
Existence of visual disturbances
Time Frame
at H0, between H0 and H0+48H
Title
Existence of lightheadedness
Time Frame
at H0, between H0 and H0+48H
Title
Existence of urinary retention
Time Frame
at H0, between H0 and H0+48H
Title
Existence of pruritus
Time Frame
at H0, between H0 and H0+48H
Title
Pain
Time Frame
at H0+0h30
Title
pain
Time Frame
at H0+1h
Title
pain
Time Frame
at H0+1h30
Title
pain
Time Frame
at H0+2h
Title
pain
Time Frame
at H0+6h
Title
pain
Time Frame
at H0+12h
Title
pain
Time Frame
at H0+24h
Title
pain
Time Frame
at H0+48h

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing a lumbar slipped disc surgery Aged 18 to 85 years. ASA score I-III Having given their consent. Affiliated with a social security scheme Exclusion Criteria: Patients who must be operated urgently. Patients previously operated for lumbar spinal surgery. Expected duration of surgery more than 3 hours. Severe renal impairment defined by a creatinine clearance less than or equal to 30 mL/min. Taking long-term strong opiates . Taking long-term corticosteroids or within 48 hours before surgery. Taking pregabalin or gabapentin within 48 hours before surgery. Drug addiction. Patients with cognitive impairment (judged by the investigator) that may interfere with: informed consent, the collection of endpoints, the use of auto-controlled analgesia. Pregnant or nursing women. Refusal of the protocol. Minor or major protected patients. Allergy or other cons-indication to the molecules used in the protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruno VERDIER
Organizational Affiliation
University Hospital, Clermont-Ferrand
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Clermont-Ferrand
City
Clermont-Ferrand
ZIP/Postal Code
63003
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
31021886
Citation
Momon A, Verdier B, Dolomie JO, Gardette M, Pereira B, Curt I, Duale C. A Single Preoperative Administration of Dexamethasone, Low-dose Pregabalin, or a Combination of the 2, in Spinal Surgery, Does Not Provide a Better Analgesia Than a Multimodal Analgesic Protocol Alone. Clin J Pain. 2019 Jul;35(7):594-601. doi: 10.1097/AJP.0000000000000719.
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Co-analgesic Effects of Dexamethasone and Pregabalin After Lumbar Slipped Disc Surgery

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