A Tolerability and Efficacy Study of TU-100 For The Treatment of Postoperative Ileus

Inclusion Criteria: In order to participate in this study, a patient must meet all of the following criteria: 1. Is at least 18 years of age; 2. Is male or female. Female patients cannot be pregnant or lactating and must be surgically sterile, postmenopausal (no menses for the previous 12 months), or practicing an effective method of birth control as determined by the investigator (eg, oral contraceptives, double barrier methods, hormonal injectable or implantable contraceptives, tubal ligation, or partner with vasectomy); 3. Has been diagnosed with sigmoid carcinoma; ascending, transverse, or descending colon carcinoma; colonic polyps; carcinoid tumors; lymphoma localized to the abdomen; ischemic bowel; toxic megacolon with no perforation; any tumor of the bowel determined to require removal; or diverticulitis; 4. Requires laparotomy for large bowel resection. Note: patients who are shifted to laparotomy during laparoscopic surgery are acceptable; 5. Is hospitalized for surgery and recovery; 6. Has a pre-operative Karnofsky performance status of 80% to 100%; and 7. Provides written informed consent prior to participation in the study after full explanations of the study purpose and procedures. Exclusion Criteria: In order to participate in this study, a patient must not meet any of the following criteria: 1. Has been diagnosed with Crohn's disease, ulcerative colitis, or irritable bowel syndrome. Note: patients with inactive ulcerative colitis who are in stable clinical remission and/or on maintenance therapy to prevent relapse are acceptable; 2. Is a pregnant or lactating female; 3. Requires a colostomy or any other ostomy device placement; 4. Requires emergency surgery or has surgery in the presence of an ongoing infection, including bowel obstruction and perforated bowel; 5. Has colorectal cancer with a Dukes Classification score of D; 6. Has diabetic neuropathy; 7. Has a history of gastroparesis; 8. Has a compromised immune system, either from treatment with corticosteroids or other immunosuppressive agents within 2 weeks of surgery or from immunosuppressive diseases (eg, human immunodeficiency virus); Note: patients on chronic treatment (for at least 3 months) with corticosteroids of up to 10 mg daily of prednisone or equivalent are acceptable if dosing has been stable for at least 2 weeks; 9. Has any other serious condition that might adversely affect their safety or ability to participate in this study, such as liver disorders (including alanine aminotransferase \[ALT\] and/or aspartate aminotransferase \[AST\] levels greater than 2.5 times the upper limit of normal \[ULN\]), kidney disorders, heart failure, blood disorders, or metabolic disorders; 10. Has a history of any allergic reactions to ginseng, ginger, Zanthoxylum fruit (Sichuan pepper), or maltose; 11. Has a history of narcotic drug abuse (especially heroin or opium) or chronic narcotic use for pain management within 2 weeks of surgery; 12. Requires anticancer radiation or chemotherapy within 2 weeks of surgery; 13. Has a history of laparotomy or laparoscopy other than simple laparoscopic procedures such as cholecystectomy, gynecological procedures, or inguinal hernia repair. Note: a history of laparoscopic fundoplication is exclusive, while a history of appendectomy or hysterectomy is acceptable; patients who have had laparotomy procedures in the past with no history of subsequent small bowel or large bowel obstruction are acceptable; 14. Has a history of any type of ileus; 15. Has a history of receiving abdominal radiation therapy in addition to subsequent small bowel or large bowel obstruction. Note: a history of radiation therapy with no small bowel or large bowel obstruction is acceptable; a history of pelvic radiation therapy is also acceptable; 16. Is unwilling or unable to comply with the procedures described in this protocol or is otherwise unacceptable for enrollment in the opinion of the investigator; and 17. Has participated in any other investigational product or device trial within 30 days prior to enrolling in this study.