WHO ICTRP trial

Efficacy of continuous preperitoneal infusion of ropivacaine in laparoscopic…

ACTRN12611000183987 · Australian New Zealand Clinical Trials Registry (ANZCTR) · Not Recruiting

Key facts

Trial ID ACTRN12611000183987
Public title Efficacy of continuous preperitoneal infusion of ropivacaine in laparoscopic colorectal surgery
Scientific title Efficacy of postoperative continuous preperitoneal infusion of 0.5% ropivacaine at 4ml/hr after laparoscopic colorectal surgery compared to intravenous patient controlled postoperative analgesia
Primary sponsor Samsung Medical Center
Secondary sponsors B. Braun Korea Co., Ltd.
Registry Australian New Zealand Clinical Trials Registry (ANZCTR)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase 4
Countries Korea, Republic Of
Conditions This study investigates postoperative analgesic efficacy and recovery in patients receiving continuous preperitoneal ropivacaine infusion vs. intravenous patient controlled analgesia after laparoscopic colorectal surgery.; This study…
Interventions Intervention consists preperitoneal placement of catheter with multiple side-holes to continuously release 0.5%ropivacaine at 4ml/hr for postoperative 72hours. This placement will be conducted by an experienced attending surgeon…
Registration date Feb 16, 2011
Target size 46
Secondary IDs Nil known
Registry page anzctr.org.au

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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