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The Effect of Remimazolam on Opioid Induced Hyperalgesia

Primary Purpose

Hyperalgesia, Mechanical

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Remimazolam
Desflurane
Remifentanil
Sponsored by
Wonkwang University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hyperalgesia, Mechanical focused on measuring remifentanil, remimazolam, opioid-induced hyperalgesia

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria will include as follows; ASA(American Society of Anesthesiologists)physical status 1-2 patients, Age with 20-65 years, and Single port-laparoscopically assisted urologic surgery. Exclusion criteria will include as follows; a known allergy to remimazolam or remifentanil, a history of drug or alcohol abuse, psychiatric disorders, acute cardiovascular disorders, or unstable hypertension, and other respiratory or neuromuscular pathology, treated with opioid-containing any analgesic drug within 24 h before surgery and contraindications to the self-administration of opioids (i.e., were unable to understand the PCA device).

Sites / Locations

  • Wonkwag UH
  • Wonkwang University hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Group DLR

Group DHR

Group RHR

Arm Description

Administer desflurane at 1 MAC, adjust the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.025 µg/kg/min.

Administer desflurane at 1 MAC, adjusting the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.3 µg/kg/min.

Administer remimazolam at a dose of 6 mg/kg/h initially, followed by 1 mg/kg/h, and remifentanil at 0.3 µg/kg/min.

Outcomes

Primary Outcome Measures

The mechanical hyperalgesia threshold
The mechanical hyperalgesia threshold (g/mm^2) (preoperative) and 2 cm from the single port incision site (postoperative) at four points (horizontally and perpendicularly).

Secondary Outcome Measures

Time to first postoperative analgesic requirement
Time to first postoperative analgesic requirement (min)
Injected PCA volume containing morphine for 24 h after surgery
Injected PCA volume containing morphine for 24 h after surgery (ml)
Pain intensity
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Pain intensity
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Pain intensity
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Pain intensity
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Area of hyperalgesia around surgical incision
Area of hyperalgesia around surgical incision (cm^2)

Full Information

First Posted
March 28, 2023
Last Updated
October 5, 2023
Sponsor
Wonkwang University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05866315
Brief Title
The Effect of Remimazolam on Opioid Induced Hyperalgesia
Official Title
The Effect of Remimazolam on Remifentanil-induced Hyperalgesia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
May 19, 2023 (Actual)
Primary Completion Date
September 6, 2023 (Actual)
Study Completion Date
September 15, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wonkwang University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this prospective, randomized, controlled study is to investigate the effect of remimazolam on opioid-induced hyperalgesia (OIH) in patients undergoing single port-laparoscopically assisted urologic surgery. The main question[s] it aims to answer are: [The mechanical hyperalgesia threshold] [Area of hyperalgesia around the surgical incision 24 h after surgery (cm^2)] In three groups: Group RHR (Remimazolam- High-dose Remifentanil), Group DHR (Desflurane-low-dose Remifentanil) or Group DLR (Control).
Detailed Description
Ninety-three (n = 31 per group) American Society of Anesthesiologists I-II patients (age 20-65 years) will be scheduled for single port-laparoscopically assisted urologic surgery. Group RHR (Remimazolam-Remifentanil): Administer remimazolam at a dose of 6 mg/kg/h initially, followed by 1 mg/kg/h, and remifentanil at 0.3 µg/kg/min. Group DHR (Desflurane-Remifentanil): Administer desflurane at 1 minimum alveolar concentration (MAC), adjusting the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.3 µg/kg/min. Group DLR (Control): Administer desflurane at 1 MAC, adjust the dose by 1 vol% titration to maintain mean arterial pressure (MAP) and bispectral index (BIS) levels, and remifentanil at 0.3 µg/kg/min. Mechanical hyperalgesia threshold, Time to first postoperative analgesic requirement (min), Injected PCA volume containing morphine for 12 h after surgery (ml), Pain intensity: VAS 1 h after surgery, VAS 6 h after surgery, VAS 12 h after surgery VAS 24 h after surgery. Area of hyperalgesia around the surgical incision 24 h after surgery (cm^2) will be checked.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperalgesia, Mechanical
Keywords
remifentanil, remimazolam, opioid-induced hyperalgesia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Group RHR (Remimazolam- High doses of Remifentanil): Administer remimazolam at a dose of 6 mg/kg/h initially, followed by 1 mg/kg/h, and remifentanil at 0.3 µg/kg/min. Group DHR (Desflurane-High doses of Remifentanil): Administer desflurane at 1 MAC, adjusting the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.3 µg/kg/min. Group DLR (Desflurane-Low-dose of Remifentanil): Administer desflurane at 1 MAC, adjust the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.025 µg/kg/min.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
A trained anesthesiologist not involved in general anesthesia assessed clinically relevant and mechanically evoked pain using the Von-Frey filaments and secondary outcomes after surgery.
Allocation
Randomized
Enrollment
108 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group DLR
Arm Type
Active Comparator
Arm Description
Administer desflurane at 1 MAC, adjust the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.025 µg/kg/min.
Arm Title
Group DHR
Arm Type
Experimental
Arm Description
Administer desflurane at 1 MAC, adjusting the dose by 1 vol% titration to maintain MAP and BIS levels, and remifentanil at 0.3 µg/kg/min.
Arm Title
Group RHR
Arm Type
Experimental
Arm Description
Administer remimazolam at a dose of 6 mg/kg/h initially, followed by 1 mg/kg/h, and remifentanil at 0.3 µg/kg/min.
Intervention Type
Drug
Intervention Name(s)
Remimazolam
Other Intervention Name(s)
Byfavo
Intervention Description
Administer remimazolam
Intervention Type
Drug
Intervention Name(s)
Desflurane
Other Intervention Name(s)
desfuralne
Intervention Description
administer desflurane
Intervention Type
Drug
Intervention Name(s)
Remifentanil
Other Intervention Name(s)
Ulitva
Intervention Description
administer remifentanil
Primary Outcome Measure Information:
Title
The mechanical hyperalgesia threshold
Description
The mechanical hyperalgesia threshold (g/mm^2) (preoperative) and 2 cm from the single port incision site (postoperative) at four points (horizontally and perpendicularly).
Time Frame
at 24 hours after surgery
Secondary Outcome Measure Information:
Title
Time to first postoperative analgesic requirement
Description
Time to first postoperative analgesic requirement (min)
Time Frame
Within 1 hour after surgery
Title
Injected PCA volume containing morphine for 24 h after surgery
Description
Injected PCA volume containing morphine for 24 h after surgery (ml)
Time Frame
24 hours after surgery
Title
Pain intensity
Description
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Time Frame
1 hour after surgery
Title
Pain intensity
Description
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Time Frame
6 hours after surgery
Title
Pain intensity
Description
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Time Frame
12 hours after surgery
Title
Pain intensity
Description
The Visual analogue scales (VAS)-100 is a line with words describing the extremes of pain from "no pain" to "worst imaginable pain".
Time Frame
24 hours after surgery
Title
Area of hyperalgesia around surgical incision
Description
Area of hyperalgesia around surgical incision (cm^2)
Time Frame
24 hours after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria will include as follows; ASA(American Society of Anesthesiologists)physical status 1-2 patients, Age with 20-65 years, and Single port-laparoscopically assisted urologic surgery. Exclusion criteria will include as follows; a known allergy to remimazolam or remifentanil, a history of drug or alcohol abuse, psychiatric disorders, acute cardiovascular disorders, or unstable hypertension, and other respiratory or neuromuscular pathology, treated with opioid-containing any analgesic drug within 24 h before surgery and contraindications to the self-administration of opioids (i.e., were unable to understand the PCA device).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cheol Lee, M.D.,Ph.D.
Organizational Affiliation
Wonkwang University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Wonkwag UH
City
Iksan
State/Province
Jeollabukdo
ZIP/Postal Code
54538
Country
Korea, Republic of
Facility Name
Wonkwang University hospital
City
Iksan
ZIP/Postal Code
54538
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Effect of Remimazolam on Opioid Induced Hyperalgesia

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