Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)

Abstract Background Cholecystectomy is the preferred treatment for symptomatic cholecystolithiasis. However, persistent pain after cholecystectomy for symptomatic cholecystolithiasis is reported in up to 40% of patients. The aim of the SECURE trial is to compare the effectiveness of usual care with...

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Main Authors: Sarah Z. Wennmacker, Aafke H. van Dijk, Joost P. H. Drenth, Sandra C. Donkervoort, Djamila Boerma, Gert P. Westert, Cornelis J. H. M. van Laarhoven, Marja A. Boermeester, Marcel G. W. Dijkgraaf, Philip R. de Reuver
Format: Article
Language:English
Published: BMC 2018-11-01
Series:Trials
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13063-018-2989-5
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spelling doaj-05392516ba674b2b9f4e681dfbb7c3e12020-11-25T01:53:19ZengBMCTrials1745-62152018-11-0119111010.1186/s13063-018-2989-5Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)Sarah Z. Wennmacker0Aafke H. van Dijk1Joost P. H. Drenth2Sandra C. Donkervoort3Djamila Boerma4Gert P. Westert5Cornelis J. H. M. van Laarhoven6Marja A. Boermeester7Marcel G. W. Dijkgraaf8Philip R. de Reuver9Department of Surgery, Radboud University Medical CentreDepartment of Surgery, Academic Medical CentreGastroenterology and Hepatology, Radboud University Medical CentreDepartment of Surgery, Onze Lieve Vrouwe GasthuisDepartment of Surgery, St. Antonius HospitalDepartment of IQ healthcare, Radboud University Medical CentreDepartment of Surgery, Radboud University Medical CentreDepartment of Surgery, Academic Medical CentreClinical Research Unit, Academic Medical CentreDepartment of Surgery, Radboud University Medical CentreAbstract Background Cholecystectomy is the preferred treatment for symptomatic cholecystolithiasis. However, persistent pain after cholecystectomy for symptomatic cholecystolithiasis is reported in up to 40% of patients. The aim of the SECURE trial is to compare the effectiveness of usual care with a restrictive strategy using a standardized work-up with stepwise selection for cholecystectomy in patients with gallstones and abdominal complaints. The SECURE trial is designed as a multicenter, randomized, parallel-arm, non-inferiority trial in patients with abdominal symptoms and ultrasound-proven gallstones or sludge. Randomization was performed to either usual care (standard practice, according to the physician’s knowledge and experience, and physician’s and patient’s preference) or a restrictive standardized strategy: treated with interval evaluation and stepwise selection for laparoscopic cholecystectomy based on fulfilment of pre-specified criteria. This article presents in detail the statistical analysis plan (SAP) of this trial and was submitted before outcomes were available to the investigators. Results The primary end point of this trial is defined as the proportion of patients being pain-free at 12 months’ follow-up. Pain will be assessed with the Izbicki Pain Score. Secondary endpoints will be the proportion of patients with complications due to gallstones or cholecystectomy, quality of life, the association between the patients’ symptoms and treatment, work performance, and cost-effectiveness. Discussion The data from the SECURE trial will provide evidence whether or not a restrictive strategy in patients with symptomatic cholecystolithiasis is associated with similar patient reported outcomes and a reduction in the number of cholecystectomies compared to usual care. The data from this trial will be analyzed according to this pre-specified SAP. Trial registration The Netherlands National Trial Register NTR4022. Registered on 5 June 2013.http://link.springer.com/article/10.1186/s13063-018-2989-5CholecystectomySymptomatic gallstonesAbdominal painCost-effectiveness
collection DOAJ
language English
format Article
sources DOAJ
author Sarah Z. Wennmacker
Aafke H. van Dijk
Joost P. H. Drenth
Sandra C. Donkervoort
Djamila Boerma
Gert P. Westert
Cornelis J. H. M. van Laarhoven
Marja A. Boermeester
Marcel G. W. Dijkgraaf
Philip R. de Reuver
spellingShingle Sarah Z. Wennmacker
Aafke H. van Dijk
Joost P. H. Drenth
Sandra C. Donkervoort
Djamila Boerma
Gert P. Westert
Cornelis J. H. M. van Laarhoven
Marja A. Boermeester
Marcel G. W. Dijkgraaf
Philip R. de Reuver
Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)
Trials
Cholecystectomy
Symptomatic gallstones
Abdominal pain
Cost-effectiveness
author_facet Sarah Z. Wennmacker
Aafke H. van Dijk
Joost P. H. Drenth
Sandra C. Donkervoort
Djamila Boerma
Gert P. Westert
Cornelis J. H. M. van Laarhoven
Marja A. Boermeester
Marcel G. W. Dijkgraaf
Philip R. de Reuver
author_sort Sarah Z. Wennmacker
title Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)
title_short Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)
title_full Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)
title_fullStr Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)
title_full_unstemmed Statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (SECURE trial)
title_sort statistical analysis plan of a randomized controlled trial to compare a restrictive strategy to usual care for the effectiveness of cholecystectomy (secure trial)
publisher BMC
series Trials
issn 1745-6215
publishDate 2018-11-01
description Abstract Background Cholecystectomy is the preferred treatment for symptomatic cholecystolithiasis. However, persistent pain after cholecystectomy for symptomatic cholecystolithiasis is reported in up to 40% of patients. The aim of the SECURE trial is to compare the effectiveness of usual care with a restrictive strategy using a standardized work-up with stepwise selection for cholecystectomy in patients with gallstones and abdominal complaints. The SECURE trial is designed as a multicenter, randomized, parallel-arm, non-inferiority trial in patients with abdominal symptoms and ultrasound-proven gallstones or sludge. Randomization was performed to either usual care (standard practice, according to the physician’s knowledge and experience, and physician’s and patient’s preference) or a restrictive standardized strategy: treated with interval evaluation and stepwise selection for laparoscopic cholecystectomy based on fulfilment of pre-specified criteria. This article presents in detail the statistical analysis plan (SAP) of this trial and was submitted before outcomes were available to the investigators. Results The primary end point of this trial is defined as the proportion of patients being pain-free at 12 months’ follow-up. Pain will be assessed with the Izbicki Pain Score. Secondary endpoints will be the proportion of patients with complications due to gallstones or cholecystectomy, quality of life, the association between the patients’ symptoms and treatment, work performance, and cost-effectiveness. Discussion The data from the SECURE trial will provide evidence whether or not a restrictive strategy in patients with symptomatic cholecystolithiasis is associated with similar patient reported outcomes and a reduction in the number of cholecystectomies compared to usual care. The data from this trial will be analyzed according to this pre-specified SAP. Trial registration The Netherlands National Trial Register NTR4022. Registered on 5 June 2013.
topic Cholecystectomy
Symptomatic gallstones
Abdominal pain
Cost-effectiveness
url http://link.springer.com/article/10.1186/s13063-018-2989-5
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