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Colectomy clinical trials

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NCT ID: NCT03552913 Recruiting - Surgery Clinical Trials

Enhanced Recovery After Surgery for Total Knee Arthroplasty, Left Colectomy and Hysterectomy

RAAC-AP
Start date: July 6, 2017
Phase:
Study type: Observational

The objective of the study is to assess retrospectively the effect of an awareness-raising phase in favour of Enhanced Recovery After Surgery across the Assistance Publique-Hopitaux Paris institution and to explore the determinants of compliance with modalities of Enhanced Recovery After Surgery. This multicenter study is performed for three types of surgery: total knee arthroplasty, left colectomy and hysterectomy.

NCT ID: NCT03367988 Recruiting - Colectomy Clinical Trials

Opioid Free Anesthesia vs. Opioid Anesthesia Techniques.

OFA vs OA
Start date: December 1, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

A comparison of post-operative opioid use in Laparoscopic Colectomy patients receiving Opioid or Opioid-free Anesthesia.

NCT ID: NCT03216239 Completed - Clinical trials for Small Intestinal Bacterial Overgrowth

SIBO & SIFO After Colectomy

Start date: February 24, 2015
Phase:
Study type: Observational

After subtotal colectomy, 40% of patients report abdominal pain, gas and diarrhea, and poor quality of life; whose etiology is unknown. The investigators determined whether small intestinal bacterial (SIBO or fungal overgrowth SIFO) could cause these sympotoms (> 1 year).

NCT ID: NCT02596516 Not yet recruiting - Colectomy Clinical Trials

A Comparison of Colonic Bile Acid Content Following Right and Left Colectomies

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

The aim of this study is to evaluate whether there is a difference in the bile acid content in the bowel in patients after right versus left colectomy. There is compelling evidence that patients under going resection of the right colon versus left coolon have a lower polyp detection rate in surveillance colonoscopies. The investigators intend to evaluate feces of patients undergoing left and right colectomies; prior to their surgery and again three and six months aftet the surgery. The investigators plan to compare the content of the different bile acids and to compare the content between the two groups.

NCT ID: NCT02543190 Completed - Colorectal Surgery Clinical Trials

System-Wide Improvement for Transitions After Surgery: The SWIFT Post op Program

SWIFT
Start date: October 2014
Phase: N/A
Study type: Interventional

Short-term post-operative complications after colon and rectal surgery present a known major clinical and financial burden for patients and hospitals. Focused efforts to reduce readmissions after colorectal surgery is one potentially high-yield and broad approach to address this problem since post- operative complications are the strongest predictor of readmissions. We focus on decreasing readmissions after ileostomy surgery by using a previously published intervention that prevents dehydration in the outpatient setting and decreases acute renal failure complications. We plan to introduce the SWIFT post op program for ileostomy patients at one academic and two community hospitals which are part of a single health care system, and to then randomize patients to usual care in the setting of this new program versus an aggressive compliance surveillance and improvement strategy (CSIS) strategy using study personnel. Our primary study outcome is all-cause 30-day readmission, and our secondary outcomes include patient satisfaction (CAHPS scores) and a cost-benefit analysis. We seek to create a partnership between colorectal surgeons, inpatient nurse managers and wound ostomy continence nurses (WOCN) at the three sites, linking them with outpatient nurse practitioners and physician's assistants at the respective colorectal surgery clinics who facilitate care-transition after hospital discharge.

NCT ID: NCT02509910 Completed - Fluid Therapy Clinical Trials

Implementation of a GDT Algorithm for Major Surgery Patients

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

This study examines the effect of an algorithm for GDT for patients undergoing major surgery under routine conditions.

NCT ID: NCT02065661 Completed - Clinical trials for Small Bowel Obstruction

Product Validation Study of 2 New Devices, EZ-NG (RightSpot pH Indicator) and EZ-pH (RightLevel pH Indicator)

Start date: September 2011
Phase: N/A
Study type: Observational

EZ Holdco Inc. has developed two devices for the measurement of gastric content pH. The devices, EZ-NG and EZ-pH, rapidly check gastric pH by aspirating gastric contents into the device through a nasogastric (NG) tube and causing a color change in the device. The color change is then compared to the reference indicator on the device to determine a pH value of the aspirate. Currently there is no bedside rapid way to check gastric pH that protects the clinician from being exposed to the aspirate. 1. Primary Objective To assess the accuracy of the pH measurement of gastric fluid on the devices by comparing the reading on the 2 devices to a standard clinically approved pH probe. 2. Secondary Objective To determine what percentage of time the EZ-NG - RightSpot pH indicator could have been used to determine proper placement of the NG tube when initially placed.

NCT ID: NCT01079442 Completed - Colectomy Clinical Trials

Coffee Trial - Does Coffee Intake Reduce Postoperative Ileus After Elective Colectomy?

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of the investigators study is to investigate the effects of coffee on the return of bowel function and appetite, length of hospital stay, and complications after elective open colectomy in a prospective randomized trial. The primary efficacy endpoint is time to first bowel movement.

NCT ID: NCT00911391 Completed - Colorectal Cancer Clinical Trials

Randomised Trial of Doppler-Optimised Fluid Balance in Elective Colectomy

Start date: November 2009
Phase: Phase 3
Study type: Interventional

Perioperative fluid management has been historically dictated by outdated, contradictory concepts. Excessive or inadequate fluid administration around surgery is deleterious and hence goal-directed fluid therapy using Oesophageal Doppler-derived cardiac indices is preferable to optimize tissue perfusion. Previous studies in this area have been hampered by lack of standardization in other aspects of perioperative care and none have explored the impact of individualized fluid therapy on post-operative fatigue.The investigators proposed a study involving 80 patients having open/ laparoscopic colonic surgery to investigate the effect of Oesophageal Doppler guided fluid administration intraoperatively compared to current best practice of fluid restriction. The investigators have an optimized peri-operative care pathway established at the Manukau Surgical Centre (MSC), Middlemore Hospital. All patients will be cared for under the Enhanced Recovery After Surgery (ERAS) multimodal care plan therefore ensuring that all other aspects of care besides intraoperative fluid administration remain homogenous. Outcomes will include post-operative recovery, clinical outcomes as well as physiological data with follow-up to 30 days.

NCT ID: NCT00888888 Completed - Appendicitis Clinical Trials

Colonic Resections in Patients With Suspected Appendicitis

Start date: April 2009
Phase: N/A
Study type: Observational

Although many reports have been published on colonic resections in patients with suspected appendicitis and the diseases that cause the decision to resect the colon have been identified and their proper treatments have been established, there is no report on the risk factors present in converting a simple appendectomy into a major colonic resection. The investigators aimed to identify the risk factors that lead the surgeon to perform a colonic resection in patients undergoing surgery for initially suspected acute appendicitis.