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Postoperative Ileus clinical trials

View clinical trials related to Postoperative Ileus.

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NCT ID: NCT02175979 Completed - Anastomotic Leak Clinical Trials

SANICS II Trial: Stimulation of the Autonomic Nervous System in Colorectal Surgery by Perioperative Nutrition

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

The main objective is to investigate the effects of perioperative nutrition on postoperative ileus and anastomotic leakage in patients undergoing colorectal surgery. Perioperative enteral nutrition is compared to the standard of care (fasting perioperatively).

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: 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.

NCT ID: NCT01710982 Completed - Postoperative Ileus Clinical Trials

A Study to Evaluate the Safety of TZP-101 (IV Ulimorelin) Administered Post-Operatively in Patients Who Have Undergone Partial Bowel Resection

Start date: February 2012
Phase: Phase 3
Study type: Interventional

A study to evaluate the safety of TZP-101 in comparison with placebo when administered post-operatively in patients who have undergone partial bowel resection.

NCT ID: NCT01699919 Completed - Postoperative Pain Clinical Trials

A Study to Assess Analgesic Efficacy of Intravenous Lignocaine

Start date: April 2011
Phase: Phase 4
Study type: Interventional

The primary objectives of this study are to analyse the effect of perioperative systemic infusion of lignocaine on postoperative pain, postoperative nausea and vomiting and perioperative levels of inflammatory mediators in patients undergoing elective open abdominal surgeries. The secondary parameters which will be observed during the study are the time to passage of flatus and stools postoperatively.

NCT ID: NCT01668199 Completed - Postoperative Ileus Clinical Trials

A Study in Healthy Male Subjects Designed to Assess the Mass Balance Recovery and Pharmacokinetics of 14C TZP-101

Start date: February 2012
Phase: Phase 1
Study type: Interventional

A study to investigate the mass balance recovery and pharmacokinetics of 14C TZP-101.