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Ileus clinical trials

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NCT ID: NCT02232893 Completed - Postoperative Ileus Clinical Trials

Effect of TU-100 in Patients Undergoing Laparoscopic Colectomy

TU100P2T3
Start date: September 2014
Phase: Phase 2
Study type: Interventional

TU-100 is a gastrointestinal drug produced from the three botanical raw materials, Asian ginseng, Zanthoxylum fruit (Japanese pepper), and ginger, based on proprietary aqueous decoction and granulation technology. The aim of this study is to assess the effect of TU-100 on post-operative quality of life during the 4 week postoperative period after straight, hand-assisted, or robot-assisted laparoscopic colectomy. Optimal efficacy parameters for subsequent outcome studies also will be explored.

NCT ID: NCT02218190 Completed - Spinal Fusion Clinical Trials

Alvimopan and Ileus in PSF

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to determine with Alvimopan reduces the incidence of post operative ileus in patients who undergo posterior spinal fusion.

NCT ID: NCT02162134 Completed - Clinical trials for Postoperative Ileus.

Does Sugared or Sugar Free Chewing Gum Reduces Postoperative Ileus After Laparoscopic Cholecystectomy

Start date: January 2013
Phase: N/A
Study type: Interventional

Laparoscopic cholecystectomy is now very common procedure to remove the gall bladder from abdomen. After this procedure many patients suffer from the non functioning of intestine and stomach which is very common after any abdominal surgery. Many efforts tried to reduce this non functioning period or postoperative ileus but non of them was superior later on. The investigators want to evaluate the role of chewing gum for reducing postoperative ileus. The investigators hypothesis is that Chewing gum after laparoscopic cholecystectomy reduces postoperative ileus and sugared preparations are more effective to reduce it.

NCT ID: NCT02161367 Completed - Postoperative Ileus Clinical Trials

Effect of Simethicone on Postoperative Ileus in Patients Undergoing Colorectal Surgery

Start date: October 2014
Phase: Phase 4
Study type: Interventional

Post-operative ileus is a common complication following abdominal surgery. It results in abdominal distension, nausea and vomiting as well as abdominal pain. Furthermore, this results in prolonged hospital stay and occasionally readmission following abdominal surgery.The etiology of post-operative ileus is multifactorial and studies evaluating potential treatment options are abundant, though few reliable interventions exist. This study proposal describes a double-blinded randomized controlled trial investigating the effect of simethicone on post-operative ileus in patients undergoing colorectal surgery.

NCT ID: NCT02155153 Completed - Postoperative Ileus Clinical Trials

Role of Chewing Gum in Reducing Post Operative Ileus After Reversal of Ileostomy

Start date: June 2014
Phase: N/A
Study type: Interventional

Postoperative ileus is generally referred to as the transient impairment of bowel motility after abdominal or other surgery and diagnosed by postoperative abdominal pain vomiting constipation and distension. The potential complications of prolonged POI include increased postoperative pain, increased nausea and vomiting, pulmonary complications, poor wound healing, delay in resuming oral intake, delay in postoperative mobilization, prolonged hospitalization, and increased health-care costs. The estimated economic impact of POI in the United States is $7.5 billion per year, excluding the expenses of work loss. In view of these complications and economic burden a number of pharmacologic and non-pharmacologic strategies have been adopted by the doctors all over the world to reduce the burden of postoperative ileus.These programs involve transverse or curved surgical incisions, removal of nasogastric tubes at the end of anesthesia, intraoperative and postoperative analgesia, early postoperative feeding, mobilization, and gum chewing. The use of gum chewing has emerged as a new and simple modality for decreasing POI. And reviews have concluded that there is consistent benefit for patients from gum chewing after the intestinal surgery; colonic surgery and gynecological surgery. This study is based on the hypothesis that postoperative gum chewing is beneficial in prevention of postoperative ileus after reversal of ileostomy.

NCT ID: NCT02004652 Completed - Postoperative Ileus Clinical Trials

Prucalopride for Postoperative Ileus in Patients Undergoing Gastrointestinal Surgery

Start date: November 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect and safety of prucalopride on recovery of gastrointestinal function in patient undergoing major gastrointestinal surgery. The investigators hypothesize that patients who take prucalopride after major gastrointestinal surgery will have shorter duration of postoperative ileus.

NCT ID: NCT01956643 Completed - Postoperative Ileus Clinical Trials

Effect of Sham Feeding on Postoperative Ileus After Elective Liver Transplantation

Start date: October 2013
Phase: N/A
Study type: Interventional

Postoperative ileus is a common after abdominal surgery. Multifactorial etiology such as surgical trauma, bowel manipulation and perioperative opioids contributes to delayed return of normal gut function Chewing gum has recently been used as a form of sham feeding to stimulate acceleration of gut function after abdominal surgery. The investigators hypothesize that sham feeding with chewing gum will accelerate return of gut function after liver transplantation.

NCT ID: NCT01943409 Completed - Cancer Clinical Trials

Intravenous Nutrition in Hospitalized Patients: Comparison of Two Oils

Start date: July 2013
Phase: Phase 4
Study type: Interventional

Intravenous nutrition is an important therapy for the recovery of many patients. It is indicated when the patients cannot take food by mouth or use their intestines for feeding. It is important to indicate it in the appropriate setting because it's not free of complications and is a costly treatment. Some of the complications are: elevated blood sugar or lipids, elevated liver function tests, infection of the catheter or device used to administer intravenous nutrition. Intravenous nutrition is composed by proteins, lipids, carbohydrates (sugar in the form of glucose) and vitamins. Until recently, Intralipid, a soybean oil-based lipid emulsion was the only lipid available in Canada for this kind of nutrition. Since 2010, a new lipid emulsion (ClinOleic) based on olive-oil has been approved by Health Canada for use in intravenous nutrition. There is an increasing need for hospitals to evaluate the quality of intravenous nutrition administered to hospitalized patients in terms of: assessing indications, prescription, complications, clinical results and costs. The objective of this study is to determine if intravenous nutrition prescribed in hospitalized patients is indicated following existing guidelines in terms of timing of nutrition support, prescription, monitoring and whether it is associated with complications. In addition, length of stay and mortality will be assessed. Also, we will evaluate nutritional, infectious and inflammatory parameters in patients receiving soybean oil-based lipid emulsion (Intralipid) compared to those of patients receiving olive oil-based lipid emulsion (ClinOleic).

NCT ID: NCT01879605 Completed - Surgery Clinical Trials

Study About Effect of Preoperative Bowel Preparation Versus no Bowel Preparation Before Spinal Surgery

Start date: December 2007
Phase: Phase 4
Study type: Interventional

This study investigated the effect of preoperative bowel preparations for patients undergoing spinal fusion surgery.

NCT ID: NCT01818375 Completed - Postoperative Ileus Clinical Trials

Goal Directed Fluid Therapy and Postoperative Ileus

Start date: February 2013
Phase: N/A
Study type: Interventional

Despite Goal Directed Fluid Therapy (GDFT) has shown a reduction of hospitalization and overall complications in patients undergoing abdominal surgery, there is a need to address the effect of implementing GDFT on the incidence of specific surgical complications and in a context of en enhanced recovery program (ERP). Specifically, studies investigating the impact of GDFT on primary postoperative ileus (POI) in patients undergoing laparoscopic colorectal surgery and using an ERP are missing. It is hypothesized that the incidence of primary POI will be reduced in patients receiving intraoperative GDFT compared to patients receiving Standard Fluid Therapy (SFT) after elective laparoscopic colorectal surgeries with an ERP program.