Modified Circumcision Using the Disposable Circumcision Suture Device in Children: A Randomized Controlled Trial.

Objective: To evaluate and compare the surgical outcomes and complications of the modified circumcision using disposable circumcision suture device (device group) and the conventional dorsal slit circumcision (conventional group) in children.

Methods: A total of 284 patients were randomized to either device group or conventional group. All patients were preoperatively assessed and evaluated at 4 weeks after surgery.