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Colon Adenoma clinical trials

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NCT ID: NCT03444090 Completed - Colon Polyp Clinical Trials

Impacts of Inspection During Instrument Insertion on Colonoscopy Quality

Start date: October 2, 2017
Phase: N/A
Study type: Interventional

Small colon polyps which are found during colonoscopy insertion are sometimes difficult to find during withdrawal and thus missed. The investigators aim to evaluate the differences of colon polyp/adenoma detection rates of patients undergoing additional inspection and polypectomy during insertion as compared to the patients undergoing traditional practice of careful inspection and polypectomy performed entirely during withdrawal of colonoscopy.

NCT ID: NCT03390907 Completed - Colon Cancer Clinical Trials

Hybrid APC Assisted EMR for Large Colon Polyps

Start date: September 28, 2018
Phase: N/A
Study type: Interventional

The purpose of this study to evaluate and examine whether use of Hybrid Argon Plasma Coagulation (APC) as an adjunct to endoscopic mucosal resection (EMR) will reduce the risk of residual or recurrent neoplasia at 6 months. Hybrid APC is an existing FDA approved device used to assist with ablation of abnormal tissue anywhere in the GI tract.

NCT ID: NCT03361904 Completed - Colon Cancer Clinical Trials

Colonoscopic Adenoma and Advanced Neoplasia Detection Rates According to Age

Start date: January 1, 2016
Phase: N/A
Study type: Observational [Patient Registry]

Current recommendations for colonoscopy screening programs usually involve patients older than 50 years of age. However, little is known about polyp or adenoma detection rates under 50. We compared these detection rates according to age in a large series of patients in common practice. Methods: All colonoscopies performed in 2016 in our unit were prospectively recorded. We determined adenoma detection rate (ADR), polyp detection rate (PDR), mean number of polyps (MNP), and advanced neoplasia detection rate (ANDR).

NCT ID: NCT03336359 Completed - Colon Adenoma Clinical Trials

Linked Color Imaging Versus Narrow Band Imaging for Colorectal Adenoma Detection

Start date: October 23, 2017
Phase: N/A
Study type: Interventional

This is a prospective randomized trial comparing the adenoma detection rate of LCI with NBI. Eligible patients are randomly allocated in a 1:1 ratio to undergo tandem colonoscopy with LCI (LCI group) or NBI (NBI group). Randomization will be carried out by computer generated random sequences and stratified according to endoscopist's experiences (experienced versus fellows) and indications of colonoscopy (symptomatic vs screening/surveillance). The primary outcome of this study is to compare the adenoma or polyp detection rates by LCI and NBI during the first examination. Secondary outcomes included adenoma/polyp miss rate by LCI or NBI. Other outcomes include sessile serrated adenomas or polyps (SSA/P) detection rates and advanced adenoma detection rates.

NCT ID: NCT03254498 Completed - Colonic Neoplasms Clinical Trials

Detection in Tandem Endocuff Cap Trial

DETECT
Start date: April 2016
Phase: N/A
Study type: Interventional

A randomised back to back study comparing cap and Endocuff to detect adenomas during colonoscopy

NCT ID: NCT02980562 Completed - Colon Adenoma Clinical Trials

Comparison of Low Volume PEG-Asc and Lower Volume PEG-Asc With Bisacodyl

Start date: May 2015
Phase: Phase 3
Study type: Interventional

Recently a low-volume polyethylene glycol containing ascorbic acid (PEG-Asc) formulation has proven as safe and effective as traditional 4-L PEG solutions for colonoscopy preparation. However, currently available aqueous purgative formulations are poorly tolerated. The aim of this study was to compare a split-dose 2-L PEG-Asc and a 1-L PEG-Asc with bisacodyl (10 mg) formulation to determine the quality of bowel cleansing and patient tolerability.

NCT ID: NCT02838888 Recruiting - Colon Adenoma Clinical Trials

Computer-assisted Detection of Colonic Polyps

KoloPol I
Start date: July 2016
Phase: N/A
Study type: Observational

Screening colonoscopy is considered the gold standard for adenoma detection in the colon. However, it has been shown that a considerable number of polyps can be missed during screening colonoscopy. Until now the endoscopist himself is responsible for the detection of adenomatous polyps. No automatic tools are available supporting the colonoscopist to detect lesions. Recently, a computer program was developed that can be used to recognize and extract suspicious structure from colonoscopy video sequences. The program was built to automatically detected colonic polyps and to highlight the polyps by colour marking. The program was now refined so that the respective structures can be highlighted during real time colonoscopy. The aim of this feasibility study is to test whether the software is applicable during real time colonoscopy.

NCT ID: NCT02819492 Completed - Colon Adenoma Clinical Trials

Side Specific Withdrawal Times for Colonoscopy: Impact on Adenoma Detection in the Proximal and Distal Colon

SNOWCAT
Start date: November 2014
Phase: N/A
Study type: Observational

Adenoma detection in the main goal of screening colonoscopy. In order to detect adenomas it is mandatory to spend a long enough time investigating the colonic mucosa. A minimum observation time of 6 minutes has been proposed as a quality criterion for screening colonoscopy. However, different locations of the colon (proximal, distal) may require specific observation time periods. The colon can be divided into a proximal (right) and distal (left) part. Until now, it is unclear whether observation time has a significant impact on adenoma detection in both parts of the colon. The aim of this study therefore is to conduct a trial in which side-specific observation times and adenoma detection rates are measured in order to investigate this correlation in particular for the right colon.

NCT ID: NCT02250196 Completed - Colorectal Cancer Clinical Trials

A Randomized Prospective Trial Comparing Low-volume Bowel Preparation Methods

Start date: March 2013
Phase: Phase 3
Study type: Interventional

Colonoscopy is a common screening method to detect polyps and CRC. With the early detection of CRC through screening colonoscopy, patients could have better therapeutic effects and outcomes. In population screening programs, an increase in completed colonoscopies is related to a decrease in mortality from CRC. However, the miss rate for detecting colorectal neoplastic polyps of colonoscopy is 5-28%. The reluctance of participants to undergo bowel preparation results in the relatively low rate of detection of polyps and CRC, because poor preparation interferes with successful colon mucosa examination during a colonoscopy. Low-volume bowel preparations provide equivalent cleansing effect compared with standard 4 liter polyethylene glycol. However, studies comparing the superiority between low-volume bowel preparations are rare, and results are controversial. This study aimed to compare the bowel cleansing quality and tolerability between split-dose sodium picosulfate/magnesium citrate and polyethylene glycol with ascorbic acid.

NCT ID: NCT02057562 Active, not recruiting - Colon Adenoma Clinical Trials

Impact of Diverticular Disease on the Detection of Colon Adenomas

DECADE
Start date: February 2014
Phase: N/A
Study type: Observational

Benign adenomas of the colon have the potential to degenerate and become malignant. Therefore adenomatous polyps should be detected and resected during colonoscopy. Factors like advanced age and male gender are associated with the detection of adenomas. The same epidemiological pattern can be found with regard to colon diverticula. Furthermore, western world countries report higher incidences of both colorectal carcinoma as well as diverticular disease. It is not known whether a correlation exists between both entities. Some recent data have postulated higher adenoma detection rates in patients with concomitant diverticular disease (Rondagh EJ et al. Eur J Gastroenterol Hepatol. 2011; 23:1050-5. Kieff BJ et al. Am J Gastroenterol 2004; 99: 2007-11). If a positive correlation could be found this would possibly affect recommendations regarding colonoscopy surveillance intervals for patients with and without diverticular disease. The investigators therefore plan to conduct the following trial.