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Stopping or maintaining oral anticoagulation in patients undergoing photoselective vaporization of the prostate (SOAP) surgery for benign prostate obstruction: study protocol for a multicentre randomized controlled trial

Authors :
Hélène Charbonneau
Marie Pasquié
Benoit Peyronnet
Aurélien Descazeaud
Nicolas Barry-Delongchamps
Emmanuel Della Negra
Romain Mathieu
Gilles Karsenty
Jean-Alexandre Long
Charles Ballereau
Abdel-Rahmène Azzouzi
Benjamin Pradère
Franck Bruyère
Georges Fournier
Souhil Lebdai
Jehanne Calves
Luc Corbel
Sébastien Vincendeau
Gaelle Fiard
Caroline Thuillier
Jean-Luc Descotes
Pierre Colin
Thibaut Culty
Audrey Hesbois
Valerie Fuzier
Nicolas Savy
Atul Pathak
Pierre Albaladejo
Charles Marc Samama
Felipe Guerrero
Vincent Misraï
Source :
Trials, Vol 19, Iss 1, Pp 1-8 (2018)
Publication Year :
2018
Publisher :
BMC, 2018.

Abstract

Abstract Background Lower urinary tract symptoms related to benign prostatic obstruction (BPO) are frequent in men aged > 50 years. Based on the use of innovative medical devices, a number of transurethral ablative techniques have recently been developed for the surgical treatment of BPO. In recent years, GreenLight photoselective vaporization of the prostate (PVP) has been considered as a non-inferior alternative to transurethral resection of the prostate. The GreenLight PVP is usually considered as an interesting surgical option for patients treated via oral anticoagulants (OACs) with regard to its haemostatic properties. The aim of this study was to assess the impact of maintaining OAC treatment in patients undergoing PVP. Methods This study is a multicentre, open-label, randomized controlled trial (RCT) designed to show the non-inferiority of PVP surgery in patients with BPO treated with OACs. This study is designed to enrol 386 OAC-treated patients (treated with vitamin K antagonists and direct oral anticoagulants) who are undergoing PVP for BPO. Patients will be randomized (1:1) to either maintain or stop OAC treatment during the perioperative course. The intervention group will maintain OAC treatment until the day before surgery and resume OAC treatment the day after surgery, whereas the control group will stop OAC treatment (with or without low-molecular-weight heparin bridging therapy) according to the anaesthesia guidelines. The primary outcome of interest to be assessed is the 30-day complications rate according to the Clavien-Dindo classification. The secondary endpoint will examine the 30-day rate of haemorrhagic and thrombotic events. This study will provide 80% power to show non-inferiority, defined as not worse than a 10% (non-inferiority margin) inferior change in the proportion of patients with good outcomes (Clavien-Dindo score

Details

Language :
English
ISSN :
17456215
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.fb2f0f9576864ddc958d30d1a53fe950
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-018-3066-9