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Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial

BACKGROUND: Postoperative pain and, in a more extended perspective, quality of recovery (QOR) should be considered the principal endpoints after day surgery. Non-steroidal anti-inflammatory drugs (NSAIDs) and paracetamol are a cornerstone of pain treatment after painful day surgery. Nevertheless, NS...

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Autores principales: Stessel, Björn, Boon, Michiel, Joosten, Elbert A., Ory, Jean-Paul, Evers, Stefan, van Kuijk, Sander M. J., Dubois, Jasperina, Hoofwijk, Daisy, Jamaer, Luc, Buhre, Wolfgang F. F. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037620/
https://www.ncbi.nlm.nih.gov/pubmed/27669689
http://dx.doi.org/10.1186/s13063-016-1586-8
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author Stessel, Björn
Boon, Michiel
Joosten, Elbert A.
Ory, Jean-Paul
Evers, Stefan
van Kuijk, Sander M. J.
Dubois, Jasperina
Hoofwijk, Daisy
Jamaer, Luc
Buhre, Wolfgang F. F. A.
author_facet Stessel, Björn
Boon, Michiel
Joosten, Elbert A.
Ory, Jean-Paul
Evers, Stefan
van Kuijk, Sander M. J.
Dubois, Jasperina
Hoofwijk, Daisy
Jamaer, Luc
Buhre, Wolfgang F. F. A.
author_sort Stessel, Björn
collection PubMed
description BACKGROUND: Postoperative pain and, in a more extended perspective, quality of recovery (QOR) should be considered the principal endpoints after day surgery. Non-steroidal anti-inflammatory drugs (NSAIDs) and paracetamol are a cornerstone of pain treatment after painful day surgery. Nevertheless, NSAIDs are not always sufficiently effective, have numerous contraindications, and consequently are not suitable in up to 25 % of all patients. Metamizole is a non-opioid compound with a favourable gastrointestinal, cardiovascular and cerebrovascular profile compared to NSAIDs. The aim of this study is to assess if a combination of metamizole and paracetamol is non-inferior to a combination of ibuprofen and paracetamol in the treatment of acute postoperative pain at home after painful day case surgery. In addition, we aim to assess and compare quality of recovery (QOR) profiles of both groups. METHODS/DESIGN: This is an investigator-initiated, double-blind, randomised controlled, non-inferiority trial. A total of 200 patients undergoing elective haemorrhoid surgery, arthroscopic shoulder or knee surgery, or inguinal hernia repair in a day care setting will be randomised to receive either a combination of metamizole and paracetamol (MP) or a combination of ibuprofen and paracetamol (IP). Participants will take study medication orally for 4 days. Primary endpoints are average postoperative pain intensity measured by an 11-point Numeric Rating Scale at postoperative day 1 and QOR profile measured by the Functional Recovery Index (FRI), the 1-item Global Surgical Recovery (GSR) index and the EuroQol (EQ-5D) questionnaire at days 1, 2, 3, 4, 7, 14 and 28 postoperatively. Secondary outcomes include compliance with study medication, adverse effects of study medication, use of rescue medication and satisfaction with study medication, surgery and hospital care and telephone follow-up. DISCUSSION: This study will provide clinical evidence on the analgesic efficacy and safety of a combination of metamizole and paracetamol in treating postoperative pain at home after painful day surgery. This study may also provide an insight into QOR profile after four different types of surgery and into the interrelationship between three different instruments used to assess QOR. TRIAL STATUS: Recruitment is currently ongoing. TRIAL REGISTRATION: European Union Clinical Trials Register 2015-003987-35. Registered 10 November 2015.
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spelling pubmed-50376202016-10-05 Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial Stessel, Björn Boon, Michiel Joosten, Elbert A. Ory, Jean-Paul Evers, Stefan van Kuijk, Sander M. J. Dubois, Jasperina Hoofwijk, Daisy Jamaer, Luc Buhre, Wolfgang F. F. A. Trials Study Protocol BACKGROUND: Postoperative pain and, in a more extended perspective, quality of recovery (QOR) should be considered the principal endpoints after day surgery. Non-steroidal anti-inflammatory drugs (NSAIDs) and paracetamol are a cornerstone of pain treatment after painful day surgery. Nevertheless, NSAIDs are not always sufficiently effective, have numerous contraindications, and consequently are not suitable in up to 25 % of all patients. Metamizole is a non-opioid compound with a favourable gastrointestinal, cardiovascular and cerebrovascular profile compared to NSAIDs. The aim of this study is to assess if a combination of metamizole and paracetamol is non-inferior to a combination of ibuprofen and paracetamol in the treatment of acute postoperative pain at home after painful day case surgery. In addition, we aim to assess and compare quality of recovery (QOR) profiles of both groups. METHODS/DESIGN: This is an investigator-initiated, double-blind, randomised controlled, non-inferiority trial. A total of 200 patients undergoing elective haemorrhoid surgery, arthroscopic shoulder or knee surgery, or inguinal hernia repair in a day care setting will be randomised to receive either a combination of metamizole and paracetamol (MP) or a combination of ibuprofen and paracetamol (IP). Participants will take study medication orally for 4 days. Primary endpoints are average postoperative pain intensity measured by an 11-point Numeric Rating Scale at postoperative day 1 and QOR profile measured by the Functional Recovery Index (FRI), the 1-item Global Surgical Recovery (GSR) index and the EuroQol (EQ-5D) questionnaire at days 1, 2, 3, 4, 7, 14 and 28 postoperatively. Secondary outcomes include compliance with study medication, adverse effects of study medication, use of rescue medication and satisfaction with study medication, surgery and hospital care and telephone follow-up. DISCUSSION: This study will provide clinical evidence on the analgesic efficacy and safety of a combination of metamizole and paracetamol in treating postoperative pain at home after painful day surgery. This study may also provide an insight into QOR profile after four different types of surgery and into the interrelationship between three different instruments used to assess QOR. TRIAL STATUS: Recruitment is currently ongoing. TRIAL REGISTRATION: European Union Clinical Trials Register 2015-003987-35. Registered 10 November 2015. BioMed Central 2016-09-26 /pmc/articles/PMC5037620/ /pubmed/27669689 http://dx.doi.org/10.1186/s13063-016-1586-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Stessel, Björn
Boon, Michiel
Joosten, Elbert A.
Ory, Jean-Paul
Evers, Stefan
van Kuijk, Sander M. J.
Dubois, Jasperina
Hoofwijk, Daisy
Jamaer, Luc
Buhre, Wolfgang F. F. A.
Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
title Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
title_full Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
title_fullStr Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
title_full_unstemmed Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
title_short Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
title_sort metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037620/
https://www.ncbi.nlm.nih.gov/pubmed/27669689
http://dx.doi.org/10.1186/s13063-016-1586-8
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