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Colorectal Disorders clinical trials

View clinical trials related to Colorectal Disorders.

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NCT ID: NCT05994326 Completed - Clinical trials for Colorectal Disorders

Perioperative Care and Short-term Outcomes of Colorectal Surgery in Addis Abeba

Start date: September 12, 2022
Phase:
Study type: Observational

Observational cohort study of adult patients undergoing colorectal surgery at Tikur Anbessa Specialized Hospital in Addis Abeba for 3 months.

NCT ID: NCT05773248 Completed - Colorectal Cancer Clinical Trials

ERAS in Colorectal Surgery: Benefits of Late Adoption

Start date: March 13, 2023
Phase:
Study type: Observational [Patient Registry]

The aim of this single-center retrospective cohort study is to explore the effect of late adaptation of an ERAS protocol in a high-volume colorectal surgical unit. The primary endpoint is the surgical outcome measured by early postoperative complications, defined by the comprehensive complications index. Secondary endpoints include amongst others LOS (length of stay), cost analysis, short-term follow-up in the ERAS group.

NCT ID: NCT05531331 Completed - Colorectal Cancer Clinical Trials

The Effect of Education on Self-Efficacy and Adaptation to Stoma of Individuals With Stoma

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of stoma care training given at home via videoconferencing after discharge on the self-efficacy and compliance with stoma of individuals with stoma. In addition to the main purpose, it is aimed to determine whether stoma care education given via video conference at home has an effect on individuals with stoma to perform their own stoma care.

NCT ID: NCT05240053 Completed - Clinical trials for Colorectal Disorders

Enhanced Recovery Program After Laparoscopic Colorectal Surgery During The Era Of COVID-19

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

The investigators included all patients who were subjected to laparoscopic colorectal surgery at investigators' center between ( December 2019 to December 2021) for benign & malignant conditions. sample size was 50 patients , divided into 2 equal groups . Group 1: included 25 patients who were subjected to enhance recovery program after laparoscopic colorectal surgery . Group 2: included 25 patients who were subjected to traditional way - nothing by mouth until the resolution of ileus, then a fluid diet, followed by a regular diet after laparoscopic colorectal surgery.

NCT ID: NCT05210647 Completed - Clinical trials for Colorectal Disorders

Robotic Assisted Colon and Rectal Surgery Prognostic and Outcome Analysis

Start date: January 1, 2019
Phase:
Study type: Observational

To analysis surgical outcome between robotic and laparoscopy colon and rectal surgery. Retrospective case-control study of single institute.

NCT ID: NCT04849702 Completed - Clinical trials for Complication of Surgical Procedure

Comparison of the Clavien-Dindo and Comprehensive Complication Index

Start date: October 20, 2012
Phase:
Study type: Observational [Patient Registry]

Our aim was to compare 2 postoperative complication scoring systems in predicting length of hospital stay and in-hospital costs after colorectal resections.

NCT ID: NCT04748744 Completed - Clinical trials for Colorectal Neoplasms

Value of Butyrylcholinesterase as a Marker of Surgical Site Infection Following Surgery for Colorectal Diseases

Start date: November 6, 2019
Phase:
Study type: Observational [Patient Registry]

Butyrylcholinesterase (BChE) is an α-glycoprotein synthesized in the liver. BchE's serum level decreases in many clinical conditions such as acute and chronic liver damage, inflammation, injury and infections, and malnutrition. The Investigators prospectively evaluate patients undergoing elective procedures for colorectal diseases. Blood samples are collected preoperatively (at day 0), post-operatively in the recovery room (day 1), and on the subsequent four days (days 2, 3, 4, and 5) for assessment of BChE, C-reactive protein, and white blood cell concentrations. The same surgical team operates all patients and is blinded to the study. Patients are monitored for post-operative infection by using standard laboratory and clinical methods. If surgical site infection (SSI) is suspected the wound is swabbed and empirical antibiotics are started. The aim of the current trial is to study whether BChE is a reliable marker for the presence of SSI in patients undergoing colorectal surgery.

NCT ID: NCT04550156 Completed - Colorectal Cancer Clinical Trials

Evaluation of the Introduction of a Colorectal Bundle in Left Sided Colorectal Resections

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

The complication rate in colorectal surgery is high and shows a large variance depending on the patient and the treating surgeon. The primary aim of the presented study is to evaluate the introduction of a colorectal bundle to reduce the complication rate in left sided colorectal resections. The colorectal bundle is a catalog of measures consisting of several items These are for example preoperative risk stratification, antibiotic and mechanical bowel preparation and preoperative showering. The primary endpoint will be the complication rate measured as the comprehensive clinical index (CCI) within 30 days. Investigators will include patients that undergo elective or emergency left sided colorectal surgery.

NCT ID: NCT04005859 Completed - Clinical trials for Colorectal Disorders

Pain Control in Colorectal Surgery: Liposomal Bupivacaine Block Versus Intravenous Lidociane

Exparel
Start date: February 22, 2018
Phase: Phase 4
Study type: Interventional

To compare the analgesic impact of intravenous perioperative lidocaine infusion with preoperative liposomal bupivacaine TAP block in colorectal surgery. This is to be integrated into the standard ERAS protocol currently utilized at Carolinas Medical Center. Primary endpoints will be postoperative pain as measured by verbal rate scale (VRS), postoperative morphine equivalents utilized per day, and over 30 days. Secondary endpoints will include date of ambulation, return of bowel function (first flatus), tolerance of goal diet, incidence of post-operative nausea and vomiting during hospital stay, length of stay (hospital and PACU), post-operative morbidity (Clavien-Dindo, related to both anesthesia and surgery), cost of hospitalization (operative, PACU, postoperative stay, and total) and quality of life on follow up.

NCT ID: NCT03995719 Completed - Surgery Clinical Trials

Educational Program for Ostomy Patients (Ostomeducat)

ostomeducat
Start date: July 1, 2014
Phase: N/A
Study type: Interventional

Stoma surgery is a relatively common treatment for patients suffering from colorectal diseases.This study aimed to investigate the impact on hospital stay and short-term overall complications prior to and following the introduction of an outpatient preoperative stoma education program.