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Adenoma Colon clinical trials

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NCT ID: NCT04654247 Completed - Adenoma Colon Clinical Trials

Endoscopic Quality Improvement System Study

Start date: April 20, 2019
Phase: N/A
Study type: Interventional

We intend to develop intelligent quality control and management software based on the work of digestive endoscopic artificial intelligence in the Department of Gastroenterology, Wuhan University Renmin Hospital, to accurately and comprehensively assess the quality of gastrointestinal endoscopy and to provide a practical basis for improving the quality of digestive endoscopy in our endoscopic center.

NCT ID: NCT04651062 Completed - Adenoma Colon Clinical Trials

Detection of Adenomas in Screening Colonoscopy

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

The Endocuff study aims to show an increase of the number of detected adenomas in screening colonoscopies when a endocuff vision (Arc Medical Design Ldt Leeds England) is used.

NCT ID: NCT04418843 Completed - Clinical trials for Colorectal Neoplasms

Cold EMR Vs Standard EMR for the Treatment of Large Nonpedunculated Homogeneous Colorectal Lesions

Start date: June 8, 2020
Phase: N/A
Study type: Interventional

This study compares the effectiveness in complete resection (absence of recurrence at 6 months) the two different techniques for performing endoscopic mucosal resection (EMR) of nonpedunculated homogeneous colorectal lesions >20mm

NCT ID: NCT03814369 Completed - Colonic Neoplasms Clinical Trials

AmplifEYE Colonoscopy vs Standard Colonoscopy

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Colonoscopy screening is proven to reduce mortality rates for colorectal cancer, which relies on early detection and removal of colonic polyps. AmplifEYE is a FDA-approved device with a row of flexible detection arms attached to the tip of colonoscope which can separate colonic folds during scope withdrawal and is believed to improve polyp detection. Real-life clinical data on this relatively new device is lacking and this study aims to compare the adenoma and polyp detection rates in AmplifEYE-assisted colonoscopy versus standard colonoscopy.

NCT ID: NCT03688906 Completed - Colo-rectal Cancer Clinical Trials

AI-EMERGE: Development and Validation of a Multi-analyte, Blood-based Colorectal Cancer Screening Test

Start date: January 12, 2018
Phase:
Study type: Observational [Patient Registry]

Freenome is using a type of artificial intelligence, called machine learning, to identify patterns of cell-free biomarkers in blood to detect cancer early. The purpose of this study is to develop and validate a blood-based assay to detect colorectal cancer by collecting blood and stool samples from healthy patients undergoing routine screening colonoscopy and from patients recently diagnosed with colorectal cancer or advanced adenomas.

NCT ID: NCT03436004 Completed - Colorectal Cancer Clinical Trials

Evaluation of Colonoscopy With a Specific Device for the Detection of Adenomas

ENDOCOLES
Start date: May 18, 2018
Phase: N/A
Study type: Interventional

Evaluation of colonoscopy with a specific device for the detection of adenomas: Multicenter, prospective and randomized study

NCT ID: NCT03274115 Completed - Adenoma Colon Clinical Trials

BLI (Blue Light Imaging) for the Histological Characterization of Colorectal Polyps

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

The accuracy of real-time histology prediction (hyperplastic vs. adenomas) of colonic polyps using white light high-definition endoscopes is suboptimal. Blue laser imaging (BLI) is a new system for image-enhanced endoscopy using laser light, that is incorporated in the last generation Fuji high- definition videocolonscopes ELUXEO. Blue laser imaging (BLI) utilizes two monochromatic lasers instead of xenon light: a 410 nm laser visualizes vascular microarchitecture, similar to narrow band imaging, and a 450 nm laser provides white light by excitation.This system should enhance the microvascular pattern of superficial lesions, making the histological prediction easier. Aim of the study is to compare the accuracy of white light and BLI systems in real-time histology prediction of colonic polyps. For this purpose all colonscopies will be performed in a standard fashion using white light. When a polyps <10mm in size will be identified, patients will be randomized in two groups. In the Group 1 (White Light Grroup), all polyps <10mm will be evaluated with white light and prediction of histology (hyperplastic versus adenomatous) will be made by means of white light. In the Group 2 (BLI Group) , all polyps <10mm in size will be evaluated with BLI and scored as hyperplastic (type 1) or adenomatous (type 2) by applying the NICE (Narrow-band Imaging International Colorectal Endoscopic) classification, indicating color/vessel/surface pattern. The level of endoscopist's confidence in predicting histology (high or low confidence) for any polyp will be also recorded. Diagnostic performances of the endoscopists (sensitivity, specificity, positive and negative predictive values) will be calculated comparing endoscopist's prediction and pathology report, considered as reference standard in both study groups in order to evaluate the accuracy of real-time histology prediction by using BLI or white light.

NCT ID: NCT03254030 Completed - Adenoma Colon Clinical Trials

Does Inspection of Colonic Mucosa During Insertion Improve Adenoma Detection?

INWARD
Start date: March 27, 2017
Phase: N/A
Study type: Interventional

This is a prospective randomised controlled trial to assess an intervention of inspection during both phases of colonoscopic examination ( insertion and withdrawal) improve adenoma detection rate when compared to inspection only during withdrawal.

NCT ID: NCT03119168 Completed - Adenoma Colon Clinical Trials

Effect of Simethicone on Screening Colonoscopy

Start date: March 15, 2017
Phase: Phase 4
Study type: Interventional

This study is evaluating the effect of adding a high dose of simethicone to the standard polyethylene glycol preparation for screening colonoscopy in the quality of the preparation , adenoma detection rate and withdrawal times.