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The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial
INTRODUCTION: So far, the recovery quality after general anesthesia is still unsatisfied. Nalmefene is a drug to treat opioid overdose and reverse opioid actions. We aim to investigate the efficacy of nalmefene on optimizing the recovery quality of patients after general anesthesia. METHODS: It is a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976492/ https://www.ncbi.nlm.nih.gov/pubmed/36859316 http://dx.doi.org/10.1186/s13063-023-07169-4 |
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author | Ma, Xiaowen Liu, Jueying Tang, Ying Lian, Qiueyue Huai, Xiaorong Liu, Wanfeng Su, Diansan |
author_facet | Ma, Xiaowen Liu, Jueying Tang, Ying Lian, Qiueyue Huai, Xiaorong Liu, Wanfeng Su, Diansan |
author_sort | Ma, Xiaowen |
collection | PubMed |
description | INTRODUCTION: So far, the recovery quality after general anesthesia is still unsatisfied. Nalmefene is a drug to treat opioid overdose and reverse opioid actions. We aim to investigate the efficacy of nalmefene on optimizing the recovery quality of patients after general anesthesia. METHODS: It is a prospective, placebo-controlled, two-arm parallel groups, multicentre, double-blind, randomized (PPPMDR) clinical trial. The participants (n = 520) will be randomly assigned into two groups. Each patient will receive either: a single dose of nalmefene 0.25 µg/kg in the intervention group, or the same volume of 0.9% NaCl solution in the control group at the end of the surgery. The primary outcome will be the time interval between the end of anaesthesia and recovery endpoints achieved (Aldrete recovery score ≥ 9) in post-anesthesia care unit (PACU). The other variables are the time interval from the end of operation to extubation; Richmond Agitation Sedation Scale (RASS) score at extubation; the time at Montreal Cognitive Assessment Scale (MoCA) orientation score ≥ 5; visual analog scale (VAS) score and adverse effects including postoperative nausea and vomiting (PONV), and pruritus in PACU and 24 h postoperatively. ANALYSIS: This trial aims to study whether small dose of nalmefene can shorten the time from the end of surgery to Aldrete score ≥ 9 and improve opioid-induced side effects.This trial focuses on providing the reliable clinical evidence for satisfactory quality of recovery. ETHICS AND DISSEMINATION: This clinical trial has been approved and supported by the ethics committee of the Renji Hospital, Shanghai Jiaotong University, School of Medicine (KY2020-150); Shanghai Tongren Hospital (2021–030-01);The First Affiliated Hospital of Guangxi Medical University (2021–032); and The First Affiliated Hospital of Zhengzhou University(2021-KY-0495–003). Analysis of the study results will be submitted to a peer-reviewed journal for publication. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04713358, Registered on September 23, 2021. |
format | Online Article Text |
id | pubmed-9976492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99764922023-03-02 The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial Ma, Xiaowen Liu, Jueying Tang, Ying Lian, Qiueyue Huai, Xiaorong Liu, Wanfeng Su, Diansan Trials Study Protocol INTRODUCTION: So far, the recovery quality after general anesthesia is still unsatisfied. Nalmefene is a drug to treat opioid overdose and reverse opioid actions. We aim to investigate the efficacy of nalmefene on optimizing the recovery quality of patients after general anesthesia. METHODS: It is a prospective, placebo-controlled, two-arm parallel groups, multicentre, double-blind, randomized (PPPMDR) clinical trial. The participants (n = 520) will be randomly assigned into two groups. Each patient will receive either: a single dose of nalmefene 0.25 µg/kg in the intervention group, or the same volume of 0.9% NaCl solution in the control group at the end of the surgery. The primary outcome will be the time interval between the end of anaesthesia and recovery endpoints achieved (Aldrete recovery score ≥ 9) in post-anesthesia care unit (PACU). The other variables are the time interval from the end of operation to extubation; Richmond Agitation Sedation Scale (RASS) score at extubation; the time at Montreal Cognitive Assessment Scale (MoCA) orientation score ≥ 5; visual analog scale (VAS) score and adverse effects including postoperative nausea and vomiting (PONV), and pruritus in PACU and 24 h postoperatively. ANALYSIS: This trial aims to study whether small dose of nalmefene can shorten the time from the end of surgery to Aldrete score ≥ 9 and improve opioid-induced side effects.This trial focuses on providing the reliable clinical evidence for satisfactory quality of recovery. ETHICS AND DISSEMINATION: This clinical trial has been approved and supported by the ethics committee of the Renji Hospital, Shanghai Jiaotong University, School of Medicine (KY2020-150); Shanghai Tongren Hospital (2021–030-01);The First Affiliated Hospital of Guangxi Medical University (2021–032); and The First Affiliated Hospital of Zhengzhou University(2021-KY-0495–003). Analysis of the study results will be submitted to a peer-reviewed journal for publication. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04713358, Registered on September 23, 2021. BioMed Central 2023-03-01 /pmc/articles/PMC9976492/ /pubmed/36859316 http://dx.doi.org/10.1186/s13063-023-07169-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Ma, Xiaowen Liu, Jueying Tang, Ying Lian, Qiueyue Huai, Xiaorong Liu, Wanfeng Su, Diansan The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
title | The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
title_full | The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
title_fullStr | The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
title_full_unstemmed | The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
title_short | The efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
title_sort | efficacy of nalmefene on anesthetic recovery of patients: a study protocol for a multicenter randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976492/ https://www.ncbi.nlm.nih.gov/pubmed/36859316 http://dx.doi.org/10.1186/s13063-023-07169-4 |
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