Randomized trial comparing low-pressure versus standard-pressure pneumoperitoneum in laparoscopic colectomy: PAROS trial

被引:7
|
作者
Celarier, S. [1 ]
Monziols, S. [2 ]
Francois, M. O. [1 ]
Assenat, V. [1 ]
Carles, P. [2 ]
Capdepont, M. [1 ]
Fleming, C. [1 ]
Rullier, E. [1 ]
Napolitano, G. [2 ]
Denost, Q. [1 ,3 ]
机构
[1] Bordeaux Univ Hosp, Dept Digest Surg, Colorectal Unit, 1 Ave Magellan, F-33600 Pessac, France
[2] Bordeaux Univ Hosp, Dept Anesthesia Ans Crit Care, 1 Ave Magellan, F-33600 Pessac, France
[3] Bordeaux Univ Hosp, Dept Digest Surg, 1 Ave Magellan, F-33600 Pessac, France
关键词
Laparoscopy; Colectomy; Low-pressure pneumoperitoneum; SIGMOID RESECTION; VALVELESS TROCAR; CLINICAL-TRIAL; COLON-CANCER; SURGERY; CHOLECYSTECTOMY; MORBIDITY;
D O I
10.1186/s13063-020-4140-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Laparoscopy, by its minimally invasive nature, has revolutionized digestive and particularly colorectal surgery by decreasing post-operative pain, morbidity, and length of hospital stay. In this trial, we aim to assess whether low pressure in laparoscopic colonic surgery (7 mm Hg instead of 12 mm Hg) could further reduce pain, analgesic consumption, and morbidity, resulting in a shorter hospital stay. Methods and analysis The PAROS trial is a phase III, double-blind, randomized controlled trial. We aim to recruit 138 patients undergoing laparoscopic colectomy. Participants will be randomly assigned to either a low-pressure group (7 mm Hg) or a standard-pressure group (12 mm Hg). The primary outcome will be a comparison of length of hospital stay between the two groups. Secondary outcomes will compare post-operative pain, consumption of analgesics, morbidity within 30 days, technical and oncological quality of the surgical procedure, time to passage of flatus and stool, and ambulation. All adverse events will be recorded. Analysis will be performed on an intention-to-treat basis.
引用
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页数:7
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