Abstract:PURPOSE:To evaluate the safety and efficacy of a new mesh in the pre-peritoneal repair of inguinal hernia.
METHODS:We randomly divided 120 patients undergoing pre-peritoneal repair into 2 groups between March 2012 and December 2013. The patients were randomized to receive the Swing mesh (n=60; study group) or the Modified Kugel mesh (n=60; control group).The primary end point of this study was to compare postoperative groin pain of the two groups. Complications, recurrence and analgesic use were also recorded.… Show more
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