Viewing Study NCT02361593



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Last Modification Date: 2024-10-26 @ 11:38 AM
Study NCT ID: NCT02361593
Status: COMPLETED
Last Update Posted: 2017-01-16
First Post: 2015-01-24

Brief Title: Transparent Cap-assisted Endoscopic Sclerotherapy
Sponsor: Shanghai Zhongshan Hospital
Organization: Shanghai Zhongshan Hospital

Study Overview

Official Title: Transparent Cap-assisted Endoscopic SclerotherapyLauromacrogol Injection in Esophageal Varices a Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2017-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study is to evaluate efficacy and safety of transparent cap-assisted endoscopic sclerotherapyIlauromacrogol injection in management of esophageal varices
Detailed Description: Endoscopic procedures now play a great role in management of esophagogastric varices Endoscopic variceal ligationEVL was recommended as first line therapy for primary and secondary prophylaxis in patients with esophageal varices Previous studies have showed a superiority of EVL over endoscopic injection of sclerotherapyEIS mainly because of lower occurrence rate of complications Procedure related complications were related to total amount of lauromacrogol number of treatment and expertise of the endoscopists Transparent cap has already been reported to assist in other endoscopic procedures such as biopsy of Barret esophagus or endoscopic submucosal dissection Accuracy and vision were improved with the help of transparent cap in the front of endoscopy We have tried transparent cap-assisted sclerotherapy in some patients with in our hospital Now a randomized controlled trial was conducted to evaluate efficacy and safety of transparent cap-assisted endoscopic sclerotherapy in management of esophageal varices

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None