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Bowel Obstruction clinical trials

View clinical trials related to Bowel Obstruction.

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NCT ID: NCT02116881 Terminated - Incisional Hernia Clinical Trials

Incisional Hernia and Adhesion-Related Bowel Obstruction

Start date: January 2015
Phase: N/A
Study type: Observational

Despite of technological advances in surgery, incisional hernia and bowel obstruction remain frequent surgical complications. To date, the relationship between these two types of surgery and the occurrence of incisional hernia remains unclear. This is an observational study to evaluate outcomes of incisional hernia with respect to the incision site and adhesion-related bowel obstruction after open and laparoscopic colorectal surgery.

NCT ID: NCT02058290 Terminated - Bowel Obstruction Clinical Trials

A Health Economic Trial in Adult Patients Undergoing Laparoscopic Colectomy

IMPROVE-Lap
Start date: December 2011
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL (bupivacaine liposome injectable suspension) to determine if total opioid consumption is reduced when using EXPAREL, therefore possibly reducing total hospital costs.

NCT ID: NCT01911793 Terminated - Ileus Clinical Trials

Stoma Tube Decompression and Postoperative Ileus After Major Colorectal Surgery

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

Postoperative ileus is common after colorectal surgery, occurring in up to 20% of patients. Stomas are frequently created in conjunction with major colorectal surgery. Obstruction at the level of the stoma is a common cause of bowel obstruction or ileus. This is often manifested by decrease or delay in stoma output and is often attributed to edema at the level of the stoma. Thus, a temporary tube (red robinson catheter) is placed into the stoma at bedside, which often relieves the obstruction until the edema at the level of the stoma resolves and stoma function occurs around the temporary tube. At this time, the tube is removed and the stoma continues to function normally. The purpose of this study is to evaluate whether a stoma tube (red-robinson catheter) placed at the time of stoma creation would reduce the incidence of postoperative ileus in patients undergoing major colorectal surgery with creation of a stoma.

NCT ID: NCT01507246 Completed - Bowel Obstruction Clinical Trials

Adult Patients Undergoing Open Colectomy MA402S23B303

IMPROVE-Open
Start date: December 2011
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL(R) to determine if total opioid consumption is reduced when using EXPAREL, therefore possibly reducing total hospitalization costs.

NCT ID: NCT01507233 Terminated - Bowel Obstruction Clinical Trials

A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B302

IMPROVE-Open
Start date: May 2012
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL (bupivacaine liposome extended-release injectable suspension) to determine if total opioid consumption is reduced when using EXPAREL, therefore possibly reducing total hospitalization costs.

NCT ID: NCT01507220 Terminated - Bowel Obstruction Clinical Trials

A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B301

IMPROVE-Open
Start date: March 2012
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL (bupivacaine liposome extended-release injectable suspension) to determine if total opioid consumption is reduced when using EXPAREL therefore possibly reducing total hospitalization costs.

NCT ID: NCT01083537 Terminated - Ovarian Cancer Clinical Trials

Trial of Best Supportive Care and Either Cisplatin or Paclitaxel to Treat Patients With Primary Ovarian Cancer, Primary Peritoneal Cancer or Fallopian Tube Cancer and Inoperable Malignant Bowel Obstruction

Start date: February 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The best way to treat MBO in patients with ovarian cancer has not been studied enough by trials that assess how more than one treatment arm (surgical, chemotherapeutic, supportive care approaches) affects clinical outcomes like resolution of bowel obstruction, survival, and quality of life. To improve patient outcomes, we must assess which patients will do better with palliative surgery, chemotherapy, or best supportive care. This study will gather safety information, and how reasonable it is to give chemotherapy and BSC to patients with advanced ovarian cancer and MBO who are non-surgical candidates. This study will also look into the effects of chemotherapy and BSC on the quality of life and resolution of bowel obstruction, in hopes to perform future studies that lead to the best management of MBO.

NCT ID: NCT01040364 Completed - Bowel Obstruction Clinical Trials

Internal Hernias After Laparoscopic Gastric Bypass

IHafterLRYGB
Start date: May 2009
Phase: N/A
Study type: Observational

The main goal of this study is to describe the trends in the incidence rate of internal hernia presentation after different modifications of the mesenteric closure technique after primary laparoscopic Roux-en-Y gastric bypass (RYGB) surgery from 1997-2009.

NCT ID: NCT00536523 Terminated - Ovarian Cancer Clinical Trials

Effect of Serotonin Level on Constipation Caused by Chemotherapy in Patients With Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

Start date: April 2007
Phase: N/A
Study type: Observational

RATIONALE: Gathering information about changes in serotonin levels in patients undergoing chemotherapy for ovarian cancer, fallopian tube cancer, or primary peritoneal cancer may help doctors learn more about constipation caused by chemotherapy. PURPOSE: This clinical trial is studying how blood levels of serotonin effect constipation caused by chemotherapy in patients with newly diagnosed ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

NCT ID: NCT00164879 Recruiting - Colorectal Cancer Clinical Trials

Endolaparoscopic Versus Immediate Surgery for Obstructing Colorectal Cancers

Start date: January 2000
Phase: Phase 3
Study type: Interventional

The aim of this study is to compare the stoma rate, clinical efficacy, and safety of patients treated by endoscopic stenting followed by elective laparoscopic resection (the 'endolaparoscopic approach') versus immediate emergency surgery for obstructing left-sided colorectal cancers.