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A Phase II Randomized Controlled Trial of Acupuncture for Reduction of Post-Colectomy Ileus

[Protocol 06-145]


Full Title :
A PHASE II RANDOMIZED CONTROLLED TRIAL OF ACUPUNCTURE FOR REDUCTION OF POST-COLECTOMY ILEUS
Purpose :

Some patients with colon cancer have an operation to remove all or part of the colon as part of their treatment, or to evaluate suspected colon cancer (a procedure called colectomy). After this type of surgery, patients' bowel function often slows down for a few days as part of the natural reaction to the surgery. It is as if the bowels "go to sleep" for a while. This condition is called "postoperative ileus." It usually lasts for a few days.

Until postoperative ileus resolves, patients may have to stay in the hospital. Being able to eat food, pass gas, and have a bowel movement are indications that postoperative ileus has resolved and that bowel function has recovered.

Postoperative ileus, as well as postoperative abdominal pain, nausea, and vomiting, can contribute to a prolonged hospital stay, hospital readmission, and complications in patients undergoing major abdominal surgery. The purpose of this study is to determine if acupuncture can help patients recover bowel function after colectomy.

Acupuncture involves the insertion of very fine needles into the skin to treat symptoms. Placebo acupuncture is a technique that looks and feels the same as acupuncture, but is thought to have a weaker effect. There is evidence suggesting that acupuncture may help reduce postoperative ileus, pain, nausea, and vomiting. In this study, patients will be randomly assigned to receive acupuncture or placebo acupuncture, and findings will be compared between the two groups.

Eligibility :

To be eligible for this study, patients must meet several criteria, including but not limited to the following:

  • Patients must be scheduled to undergo open abdominal surgery to remove all or part of the colon at Memorial Sloan-Kettering Cancer Center as treatment for colon cancer or to evaluate suspected colon cancer.
  • Patients must be age 18 or older.

For more information and to see if you are eligible for this study, please contact Dr. Gary Deng at 646-888-0841 or Derek Woo, Research Study Assistant, at 646-888-0809.

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