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

Overview of attention for article published in Trials, September 2016
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Title
Metamizole versus ibuprofen at home after day surgery: study protocol for a randomised controlled trial
Published in
Trials, September 2016
DOI 10.1186/s13063-016-1586-8
Pubmed ID
Authors

Björn Stessel, Michiel Boon, Elbert A. Joosten, Jean-Paul Ory, Stefan Evers, Sander M. J. van Kuijk, Jasperina Dubois, Daisy Hoofwijk, Luc Jamaer, Wolfgang F. F. A. Buhre

Abstract

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. 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. 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. Recruitment is currently ongoing. European Union Clinical Trials Register 2015-003987-35 . Registered 10 November 2015.

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Mendeley readers

The data shown below were compiled from readership statistics for 105 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Switzerland 1 <1%
Unknown 104 99%

Demographic breakdown

Readers by professional status Count As %
Student > Master 18 17%
Student > Bachelor 15 14%
Student > Doctoral Student 8 8%
Researcher 7 7%
Student > Postgraduate 6 6%
Other 20 19%
Unknown 31 30%
Readers by discipline Count As %
Medicine and Dentistry 42 40%
Nursing and Health Professions 6 6%
Pharmacology, Toxicology and Pharmaceutical Science 5 5%
Psychology 3 3%
Engineering 2 2%
Other 8 8%
Unknown 39 37%