This study is currently not recruiting participants.

A Phase 3 Randomized Double-blind Placebo-controlled Study to Investigate the Efficacy and Safety of the XaraColl? Bupivacaine Implant (300 mg Bupivacaine Hydrochloride) After Open Laparotomy Hernioplasty

  • STATUS
    Not Recruiting
Updated on 19 February 2024

Summary

The purpose of this study is to compare the analgesic effect of XaraColl to that with the placebo-sponge for the management of acute postoperative pain after open laparotomy inguinal hernioplasty.

Description

The purpose of this study is to compare the analgesic effect of XaraColl to that with the placebo-sponge for the management of acute postoperative pain after open laparotomy inguinal hernioplasty.

Details
Condition inguinal hernia
Age 100years or below
Clinical Study IdentifierTX5771
Last Modified on19 February 2024

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