Clinical Trials Logo

Ileus clinical trials

View clinical trials related to Ileus.

Filter by:

NCT ID: NCT02480361 Completed - Ileus Clinical Trials

Effect of Acupuncture on Postoperative Ileus After Gastric Surgery (EAPIG)

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

Postoperative ileus (POI) is a common problem after major abdominal surgery. Acupuncture is being accepted in the West as a treatment option for managing POI and various functional gastrointestinal disorders. Therefore, we conducted a prospective randomized pilot study to evaluate the effect of electro-acupuncture on POI and other surgical outcomes in patients who underwent gastric surgery for a later large-scale study.

NCT ID: NCT02469441 Completed - Postoperative Ileus Clinical Trials

Does Coffee Intake Reduce Postoperative Ileus After Elective Colorectal Surgery

COFFEE
Start date: August 1, 2014
Phase: N/A
Study type: Observational

The aim of the study is to investigate if postoperative coffee intake decreases the time until first bowel movement in elective colorectal surgery with primary anastomosis.

NCT ID: NCT02425774 Recruiting - Postoperative Ileus Clinical Trials

Anti-inflammatory Effect of Pre-operative Stimulation of the Cholinergic Anti-Inflammatory Pathway

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

Hypothesis: Prucalopride can mimic electrical stimulation of the abdominal vagus nerve and has an anti-inflammatory effect. Aims: In the present pilot study, the investigators want to evaluate the anti-inflammatory effect of prucalopride. The following aims are formulated: 1. to show that prucalopride has a similar inflammatory effect as abdominal vagus nerve stimulation (VNS) 2. to evaluate whether prucalopride leads to accelerated post-operative recovery

NCT ID: NCT02399605 Active, not recruiting - Ileus Clinical Trials

Subcutaneous Electrical Stimulation in the Prevention of Postoperative Ileus

SESPI
Start date: March 2015
Phase: N/A
Study type: Interventional

Assess whether the application of electrical stimulation in patients undergoing subcutaneous colon cancer in a Multimodal Rehabilitation Program (Fast track) decreases the incidence of postoperative ileus, improving the results of morbidity and mortality, hospitalization and health care costs.

NCT ID: NCT02329912 Recruiting - Postoperative Ileus Clinical Trials

Postoperative Ileus: Duration and Severity Assessment With the SmartPill®

PIDuSA
Start date: December 2014
Phase: N/A
Study type: Interventional

Postoperative ileus (POI) is a frequent complication after abdominal surgery leading to nausea, vomiting and infectious complications. Bowel dysmotility can last for days and necessitates parenteral nutrition resulting in an prolonged hospital stay and a high economic burden. Until now there is no evidence based therapy of manifest POI because of missing valid surrogate markers demonstrating the severity and resolution of POI. A novel tool to examine gastrointestinal function is the SmartPill®. By measuring pH value, temperature and intraluminal pressure the capsule is able to analyse gastric emptying, small bowel transit, large bowel transit and peristaltic activity. Unfortunately the use of the SmartPill® is not allowed in the first three months after abdominal surgery. Therefore a trial is needed to investigate the behaviour of the SmartPill® during its passage through the human gastrointestinal tract immediately after surgery. The primary endpoint is - to investigate the safety of the SmartPill® in patients after abdominal surgery. The secondary endpoints are: - is the SmartPill® able to detect the gastrointestinal transit and the peristaltic activity followed by abdominal surgery compared with patients which underwent thoracic/vascular surgery. - is it possible to correlate the measured parameters (delayed gastrointestinal transit, lack of peristalsis) with the clinical signs of POI (nausea, vomiting, prolonged duration until first postoperative defecation). - is the detected peristaltic activity influenced by intravenous applicated prokinetic drugs - is the detected peristaltic activity influenced by physiotherapy Using those endpoints the investigators hope to demonstrate the safety of the SmartPill® after abdominal surgery, to evaluate its ability to analyse severity and length of POI and to examine whether the used prokinetic drugs and postoperative mobilization are able to influence peristaltic activity.

NCT ID: NCT02319512 Terminated - Postoperative Ileus Clinical Trials

Effects of Chewing Gum Against Postoperative Ileus

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

The purpose of this study is to determine whether the use of chewing gum effects postoperative ileus after pancreaticoduodenectomy.

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.