Prospective, Multicenter, Randomized Controlled Study to Evaluate the Effect of INTERCEED™

Stopped The study was terminated because the pre-specified study stopping criterion has been met.

Conditions

• Subjects Scheduled to Undergo Laparoscopic Radical Resection of Rectal Carcinoma With Preventive Ileostomy

Interventions

• DEVICE: INTERCEED™
• DEVICE: Placebo

Sponsor

Ethicon, Inc.