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Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis
BACKGROUND: Acute pancreatitis is the most common complication of diagnostic and therapeutic endoscopic retrograde cholangiopancreatography (ERCP). In spite of continuing research, no pharmacologic agent capable of effectively reducing the incidence of ERCP-induced pancreatitis has found its way int...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599317/ https://www.ncbi.nlm.nih.gov/pubmed/23320650 http://dx.doi.org/10.1186/1471-230X-13-11 |
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author | Fluhr, Gabriele Mayerle, Julia Weber, Eckhard Aghdassi, Ali Simon, Peter Gress, Thomas Seufferlein, Thomas Mössner, Joachim Stallmach, Andreas Rösch, Thomas Müller, Martina Siegmund, Britta Büchner-Steudel, Petra Zuber-Jerger, Ina Kantowski, Marcus Hoffmeister, Albrecht Rosendahl, Jonas Linhart, Thomas Maul, Jochen Czakó, László Hegyi, Péter Kraft, Matthias Engel, Georg Kohlmann, Thomas Glitsch, Anne Pickartz, Tilman Budde, Christoph Nitsche, Claudia Storck, Kirsten Lerch, Markus M |
author_facet | Fluhr, Gabriele Mayerle, Julia Weber, Eckhard Aghdassi, Ali Simon, Peter Gress, Thomas Seufferlein, Thomas Mössner, Joachim Stallmach, Andreas Rösch, Thomas Müller, Martina Siegmund, Britta Büchner-Steudel, Petra Zuber-Jerger, Ina Kantowski, Marcus Hoffmeister, Albrecht Rosendahl, Jonas Linhart, Thomas Maul, Jochen Czakó, László Hegyi, Péter Kraft, Matthias Engel, Georg Kohlmann, Thomas Glitsch, Anne Pickartz, Tilman Budde, Christoph Nitsche, Claudia Storck, Kirsten Lerch, Markus M |
author_sort | Fluhr, Gabriele |
collection | PubMed |
description | BACKGROUND: Acute pancreatitis is the most common complication of diagnostic and therapeutic endoscopic retrograde cholangiopancreatography (ERCP). In spite of continuing research, no pharmacologic agent capable of effectively reducing the incidence of ERCP-induced pancreatitis has found its way into clinical practise. A number of experimental studies suggest that intrapancreatic calcium concentrations play an important role in the initiation of intracellular protease activation, an initiating step in the course of acute pancreatitis. Magnesium can act as a calcium-antagonist and counteracts effects in calcium signalling. It can thereby attenuate the intracellular activation of proteolytic digestive enzymes in the pancreas and reduces the severity of experimental pancreatitis when administered either intravenously or as a food supplement. METHODS: We designed a randomized, double-blind, placebo-controlled phase III study to test whether the administration of intravenous magnesium sulphate before and after ERCP reduces the incidence and the severity of post-ERCP pancreatitis. A total of 502 adult patients with a medical indication for ERCP are to be randomized to receive either 4930 mg magnesium sulphate (= 20 mmol magnesium) or placebo 60 min before and 6 hours after ERCP. The incidence of clinical post-ERCP pancreatitis, hyperlipasemia, pain levels, use of analgetics and length of hospital stay will be evaluated. CONCLUSIONS: If magnesium sulphate is found to be effective in preventing post-ERCP pancreatitis, this inexpensive agent with limited adverse effects could be used as a routine pharmacological prophylaxis. TRIAL REGISTRATION: Current Controlled Trials ISRCTN46556454 |
format | Online Article Text |
id | pubmed-3599317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35993172013-03-17 Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis Fluhr, Gabriele Mayerle, Julia Weber, Eckhard Aghdassi, Ali Simon, Peter Gress, Thomas Seufferlein, Thomas Mössner, Joachim Stallmach, Andreas Rösch, Thomas Müller, Martina Siegmund, Britta Büchner-Steudel, Petra Zuber-Jerger, Ina Kantowski, Marcus Hoffmeister, Albrecht Rosendahl, Jonas Linhart, Thomas Maul, Jochen Czakó, László Hegyi, Péter Kraft, Matthias Engel, Georg Kohlmann, Thomas Glitsch, Anne Pickartz, Tilman Budde, Christoph Nitsche, Claudia Storck, Kirsten Lerch, Markus M BMC Gastroenterol Study Protocol BACKGROUND: Acute pancreatitis is the most common complication of diagnostic and therapeutic endoscopic retrograde cholangiopancreatography (ERCP). In spite of continuing research, no pharmacologic agent capable of effectively reducing the incidence of ERCP-induced pancreatitis has found its way into clinical practise. A number of experimental studies suggest that intrapancreatic calcium concentrations play an important role in the initiation of intracellular protease activation, an initiating step in the course of acute pancreatitis. Magnesium can act as a calcium-antagonist and counteracts effects in calcium signalling. It can thereby attenuate the intracellular activation of proteolytic digestive enzymes in the pancreas and reduces the severity of experimental pancreatitis when administered either intravenously or as a food supplement. METHODS: We designed a randomized, double-blind, placebo-controlled phase III study to test whether the administration of intravenous magnesium sulphate before and after ERCP reduces the incidence and the severity of post-ERCP pancreatitis. A total of 502 adult patients with a medical indication for ERCP are to be randomized to receive either 4930 mg magnesium sulphate (= 20 mmol magnesium) or placebo 60 min before and 6 hours after ERCP. The incidence of clinical post-ERCP pancreatitis, hyperlipasemia, pain levels, use of analgetics and length of hospital stay will be evaluated. CONCLUSIONS: If magnesium sulphate is found to be effective in preventing post-ERCP pancreatitis, this inexpensive agent with limited adverse effects could be used as a routine pharmacological prophylaxis. TRIAL REGISTRATION: Current Controlled Trials ISRCTN46556454 BioMed Central 2013-01-15 /pmc/articles/PMC3599317/ /pubmed/23320650 http://dx.doi.org/10.1186/1471-230X-13-11 Text en Copyright ©2013 Fluhr et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Study Protocol Fluhr, Gabriele Mayerle, Julia Weber, Eckhard Aghdassi, Ali Simon, Peter Gress, Thomas Seufferlein, Thomas Mössner, Joachim Stallmach, Andreas Rösch, Thomas Müller, Martina Siegmund, Britta Büchner-Steudel, Petra Zuber-Jerger, Ina Kantowski, Marcus Hoffmeister, Albrecht Rosendahl, Jonas Linhart, Thomas Maul, Jochen Czakó, László Hegyi, Péter Kraft, Matthias Engel, Georg Kohlmann, Thomas Glitsch, Anne Pickartz, Tilman Budde, Christoph Nitsche, Claudia Storck, Kirsten Lerch, Markus M Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis |
title | Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis |
title_full | Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis |
title_fullStr | Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis |
title_full_unstemmed | Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis |
title_short | Pre-Study protocol MagPEP: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ERCP pancreatitis |
title_sort | pre-study protocol magpep: a multicentre randomized controlled trial of magnesium sulphate in the prevention of post-ercp pancreatitis |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599317/ https://www.ncbi.nlm.nih.gov/pubmed/23320650 http://dx.doi.org/10.1186/1471-230X-13-11 |
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