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Effect of Remimazolam on Postoperative Nausea and Vomiting

Primary Purpose

Postoperative Nausea and Vomiting

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Remimazolam
Control
Sponsored by
Inje University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Postoperative Nausea and Vomiting

Eligibility Criteria

19 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • women undergoing laparoscopic cholecystectomy under general anesthesia.

Exclusion Criteria:

  • moderate to severe liver dysfunction (total bilirubin ≧ 3.0 mg/dL / aspartate aminotransferase(AST) or alanine aminotransferase(ALT) ≧ 2.5 times more than normal range)
  • moderate to severe renal dysfunction (serum creatinine ≧ 2.0 mg/dL / end-stage renal disease undergoing hemodialysis)
  • tolerance to benzodiazepines
  • hypersensitivity to anesthetic drugs (Benzodiazepines, Propofol, Remifentanil, Fentanyl citrate, Rocuronium bromide, Flumazenil)
  • acute angle glaucoma
  • alcohol dependence
  • Galactose intolerance, Lactase deficiency, glucose-galactose malabsorption
  • pregnant, breast feeding women
  • BMI >35 kg/m2
  • uncontrolled diabetes mellitus

Sites / Locations

  • Sanggye Paik hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Remimazolam group

Control group

Arm Description

Remimazolam is started during induction of anesthesia at the rate of 0.3 mg/kg/hr and stopped 20 minutes before end of operation.

0.9% normal saline is started during induction of anesthesia at the rate of 0.3 ml/kg/hr and stopped 20 minutes before end of operation.

Outcomes

Primary Outcome Measures

postoperative nausea and vomit within 24 hours after the end of operation
Nausea is evaluated using 11-point verbal numeric rating scale (VNRS -none:0, mild: 1-3, moderate:4-6, severe 7-10). Vomiting is checked when the patient has vomited or has retching symptom.

Secondary Outcome Measures

quality of recovery (QoR-15) 24 hours after the end of the operation
QoR-15 survey is performed 24 hours after the end of the operation.
pain 24 hours after the end of the operation
pain is evaluated using Numeric rating scale (NRS).

Full Information

First Posted
June 27, 2022
Last Updated
July 26, 2023
Sponsor
Inje University
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1. Study Identification

Unique Protocol Identification Number
NCT05439057
Brief Title
Effect of Remimazolam on Postoperative Nausea and Vomiting
Official Title
Effect of Remimazolam on Postoperative Nausea and Vomiting in Patients Undergoing Laparoscopic Cholecystectomy
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 13, 2022 (Actual)
Primary Completion Date
April 12, 2024 (Anticipated)
Study Completion Date
April 12, 2024 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The present trial is to study the effect of low dose remimazolam on postoperative nausea and vomiting (PONV) in patients at risks of PONV (women, postoperative use of opioid, nonsmokers) undergoing laparoscopic cholecystectomy.
Detailed Description
Postoperative nausea and vomiting (PONV) is a common complication in patients undergoing general anesthesia. It is reported that PONV is observed in 50% of patients 24 hours after general anesthesia and upto 80% in high risk patients. The patients experiencing PONV may experience severe discomfort that it is important to prevent PONV. There are several prophylactic agents for PONV. 5 serotonin receptor antagonist(5-HT3 antagonist) is the most commonly used agent and other agents such as corticosteroid, neurokinin-1 receptor antagonist can also be used. Previous studies have reported the efficacy of benzodiazepine(midazolam) in a low targeting dose as a prophylactic agent of PONV. The efficacy of low dose remimazolam (short acting benzodiazepine) on PONV has not been evaluated. According to Fourth consensus guideline for the management of postoperative nausea and vomiting (2020), three prophylactic anti-emetics are recommended for patients with three or more of the risk factors of PONV. As the patients included in our study have three or more of risk factors of PONV (women, postoperative use of opioid, nonsmokers), three prophylactic anti-emetics are recommended. Our center has routinely been using 5-HT3 receptor antagonist (ramosetron) and corticosteroid (dexamethasone) for women undergoing laparoscopic cholecystectomy. However, we still find many patients complaining nausea and vomiting after operation. Therefore, we are willing to investigate the low supplemental dose of remimazolam on the prophylaxis of PONV.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Nausea and Vomiting

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
108 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Remimazolam group
Arm Type
Experimental
Arm Description
Remimazolam is started during induction of anesthesia at the rate of 0.3 mg/kg/hr and stopped 20 minutes before end of operation.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
0.9% normal saline is started during induction of anesthesia at the rate of 0.3 ml/kg/hr and stopped 20 minutes before end of operation.
Intervention Type
Drug
Intervention Name(s)
Remimazolam
Other Intervention Name(s)
remimazolam group
Intervention Description
Remimazolam is infused at a rate of 0.3 mg/kg/hr from induction of anesthesia until 20 minutes before the end of operation.
Intervention Type
Drug
Intervention Name(s)
Control
Other Intervention Name(s)
control group
Intervention Description
Normal saline is infused at a rate of 0.3 ml/kg/hr from induction of anesthesia until 20 minutes before the end of operation.
Primary Outcome Measure Information:
Title
postoperative nausea and vomit within 24 hours after the end of operation
Description
Nausea is evaluated using 11-point verbal numeric rating scale (VNRS -none:0, mild: 1-3, moderate:4-6, severe 7-10). Vomiting is checked when the patient has vomited or has retching symptom.
Time Frame
Upto 24 hours after surgery
Secondary Outcome Measure Information:
Title
quality of recovery (QoR-15) 24 hours after the end of the operation
Description
QoR-15 survey is performed 24 hours after the end of the operation.
Time Frame
Upto 24 hours after surgery
Title
pain 24 hours after the end of the operation
Description
pain is evaluated using Numeric rating scale (NRS).
Time Frame
Upto 24 hours after surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: women undergoing laparoscopic cholecystectomy under general anesthesia. Exclusion Criteria: moderate to severe liver dysfunction (total bilirubin ≧ 3.0 mg/dL / aspartate aminotransferase(AST) or alanine aminotransferase(ALT) ≧ 2.5 times more than normal range) moderate to severe renal dysfunction (serum creatinine ≧ 2.0 mg/dL / end-stage renal disease undergoing hemodialysis) tolerance to benzodiazepines hypersensitivity to anesthetic drugs (Benzodiazepines, Propofol, Remifentanil, Fentanyl citrate, Rocuronium bromide, Flumazenil) acute angle glaucoma alcohol dependence Galactose intolerance, Lactase deficiency, glucose-galactose malabsorption pregnant, breast feeding women BMI >35 kg/m2 uncontrolled diabetes mellitus
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
In-Jung Jun
Phone
82-10-9312-0162
Email
christine17@hanmail.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
In-Jung Jun, MD.PhD.
Organizational Affiliation
Associate professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sanggye Paik hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
In-Jung Jun
Phone
82-10-9312-0162
Email
christine17@hanmail.net

12. IPD Sharing Statement

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Effect of Remimazolam on Postoperative Nausea and Vomiting

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