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Colonic Polyps clinical trials

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NCT ID: NCT01979458 Completed - Colonic Polyps Clinical Trials

Photometric Stereo Endoscopy (PSE) as a Tool for Imaging the Rectum and Colon

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

The goal of this research is to assess photometric stereo endoscopy (PSE) as an endoscopic imaging technique. Specifically, topographical surface contrast reconstructed from the PSE data will be compared to conventional imaging contrast to assess if PSE provides enhanced contrast of abnormal tissue.

NCT ID: NCT01901510 Completed - Colonic Polyps Clinical Trials

Panchromoendoscopy Using Oral Indigo Carmine Mixed With Polyethylene Glycol Prep

Start date: May 2013
Phase: Phase 1
Study type: Interventional

This study first is designed to see what dose of indigo carmine ingested orally mixed with the standard colonoscopy prep is needed to provide adequate staining of the right colon. It then will use this adequate staining concentration of Indigo Carmine to study whether this dye will increase the detection of polyps during colonoscopy.

NCT ID: NCT01877525 Completed - Clinical trials for Benign Polyps of Large Intestine

Resect and Discard Approach to Diminutive Colonic Polyps

RD
Start date: October 2011
Phase: N/A
Study type: Observational

Resect and discard (RD) is a new paradigm for management of diminutive colorectal polyps wherein histology is determined by real-time endoscopic imaging; polyps are then resected and discarded rather than sent for histopathological review. The aims of this study were to compare the surveillance recommendations between RD and the standard of care where polyps are sent for histopathological review in a mixed setting of academic and community gastroenterologists and to evaluate the diagnostic performance of an RD program for management of diminutive polyps.

NCT ID: NCT01761279 Completed - Colonic Polyps Clinical Trials

High Definition Endoscopy With i-Scan for Small Colonic Polyp Evaluation: The HiScope Study

HiSCOPE
Start date: May 2011
Phase: N/A
Study type: Observational

Current standard practice is to remove all colonic polyps found during colonoscopy as it has not been possible to distinguish between polyps with some malignant potential (adenomatous) and those with negligable malignant potential (non-adenomatous). Recent advances in endoscope imaging and technology have allowed endoscopists to distinguish between these two types of polyps by examining minute surface details. i-Scan is a new digital enhancement method that aims to enhance surface details and may enable similar accurate distinction between adenomatous and non-adenomatous polyps. Hypothesis: High definition white light endoscopy plus i-Scan improves diagnostic accuracy of in-vivo assessment of colonic polyps <10mm in size over high definition white light endoscopy alone.

NCT ID: NCT01735786 Completed - Colonic Polyps Clinical Trials

EndoClot for Preventing Rebleeding After Endoscopic Mucosal Resection (EMR)

Start date: April 2010
Phase: N/A
Study type: Observational

Endoscopic mucosal resection (EMR) has been widely used as a diagnostic and treatment techniques of gastrointestinal small lesions. Postoperative rebleeding is one of the common complication following EMR. Several endoscopic hemostasis methods are currently in use. EndoClot® absorbable polysaccharide hemostat (PAPH) as a new hemostasis material was previously used for surgical hemostasis, but the therapeutic effect and safety in endoscopic application remains unknown. This study has been designed to observe the effect of rebleeding prevention after EMR.

NCT ID: NCT01712048 Completed - Colonic Polyps Clinical Trials

Submucosal Injection EMR vs. Underwater EMR for Colorectal Polyps

IvU
Start date: September 2012
Phase: N/A
Study type: Interventional

The aim of this study is to compare the efficacy and safety of two standard methods of polypectomy (polyp removal), submucosal injection-assisted endoscopic mucosal resection (EMR) and full water emersion (without submucosal injection) EMR, for large colorectal polyps.

NCT ID: NCT01665898 Completed - Colon Polyps Clinical Trials

Comparing Cold Biopsy Forceps Versus Cold Snare Biopsy for Colon Polyps

Start date: August 2012
Phase: N/A
Study type: Interventional

Comparing the efficacy of cold biopsy forceps versus cold snare biopsy for removing colon polyps.

NCT ID: NCT01638091 Completed - Colonic Polyps Clinical Trials

Practice-Based Learning to Predict Polyp Histology at Colonoscopy

Start date: March 2011
Phase: N/A
Study type: Interventional

Most colorectal cancers arise from polyps. Most polyps removed at colonoscopy are small. New technologies such as narrowband imaging (NBI) offer the possibility of in differentiation between precancerous and unimportant small polyps. Use of these technologies could decrease the costs and potentially the risks of screening and surveillance colonoscopy. Multiple studies have demonstrated the ability of experienced endoscopists to achieve high accuracy in differentiating polyp types using NBI. The investigators hypothesize that community-based endoscopists can learn to identify polyp type at colonoscopy with the aid of NBI through the use of an introductory didactic program, followed by practice based-learning, and that their experience can serve as guidelines for wider dissemination. The purpose of this study is to test an educational program combining a didactic program followed by practice-based learning that is designed to allow community-based endoscopists to become proficient at the use of NBI in the colon. This study will not affect the care of patients in any way. The research subjects will be the endoscopists, who will perform colonoscopy and polyp removal in the usual clinical fashion, with the addition of attempting to predict polyp type before resection.

NCT ID: NCT01533090 Completed - Clinical trials for Inflammatory Bowel Disease

Evaluation of Reduced-volume PEG Bowel Preparation Administered the Same Day of Colonoscopy

LowVolumePEG
Start date: April 2010
Phase: N/A
Study type: Interventional

The conventional total dose of 4 L of polyethylene glycol (PEG) given the day before the procedure is safe and effective. It has been the standard cleansing regimen for the last 25 years. To overcome the difficulty in completing the bowel preparation due to large volume and/or taste, reduced-volume (mixed) bowel preparation of bisacodyl and 2 L of PEG have been shown to provide adequate colon cleansing and better tolerability. LoVol-esse is a reduced-volume PEG-based bowel preparation to be used in combination with bisacodyl and designed to improve patient tolerability and attitude toward bowel cleansing prior to colonoscopy thanks to the reduced volume and improved taste. The present study is intended to compare the new dosing regimen of the bowel lavage solution given the same day compared with standard PEG formulation (SELG 1000) given the day before colonoscopy.

NCT ID: NCT01496781 Completed - Colonic Polyps Clinical Trials

EndoClot for Hemostasis and Preventing Post-procedure Bleeding After Endoscopic Mucosal Resection

EMR
Start date: April 2010
Phase: N/A
Study type: Interventional

Endoscopic mucosal resection (EMR) has been widely used as a diagnostic and treatment techniques of gastrointestinal small lesions. Para-procedure bleeding is one of the common complication following EMR. Several endoscopic hemostasis methods are currently in use including metallic hemoclip. EndoClot® absorbable polysaccharide hemostat (PAPH) as a new hemostasis material was previously used for surgical hemostasis, but the therapeutic effect and safety in endoscopic application remains unknown. This randomized controlled study has been designed to compare PAPH with metallic hemoclip in their hemostatic effect of intra-procedure bleeding control and rebleeding prevention during and after EMR.