Ignite Creation Date:
2024-05-06 @ 1:03 PM
Last Modification Date:
2024-10-26 @ 1:08 PM
Study NCT ID:
NCT03917056
Status:
RECRUITING
Last Update Posted:
2024-04-02
First Post:
2019-04-12
Brief Title:
Cap-assisted Endoscopic Sclerotherapy for Internal Hemorrhoids and Rectal Prolapse
Sponsor:
The Second Hospital of Nanjing Medical University
Organization:
The Second Hospital of Nanjing Medical University
Study Overview
Official Title:
Cap-assisted Endoscopic Sclerotherapy for Internal Hemorrhoids and Rectal Prolapse a Nationwide Multicenter Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-04
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:
This clinical trial aims to evaluate the efficacy and safety of long needle and short needle in the treatment of internal hemorrhoids and rectal prolapse through CAES Cap-assisted endoscopic sclerotherapy
Detailed Description:
Traditional endoscopic sclerotherapy for internal hemorrhoids require retroflection of the endoscope Retroflection of the endoscope has blind areas and affects the precise operation And short-needle injection can easily lead to artificial ulcer and secondary bleeding CAES is a new minimally invasive endoscopic technique for the treatment of internal hemorrhoids and rectal prolapse CAES was performed based on the requirement of the cap endoscope disposable endoscopic long injection needle enough insufflated air and sclerosing agent It can accurately control the injection angle direction and depth under direct vision and avoid iatrogenic injury caused by ectopic injection to the greatest possible extent To investigate the effect of long needle and short needle on the outcome of CAES participants with internal hemorrhoids and rectal prolapse were randomly assigned to a long needle group and a short needle group using a prospective randomized controlled study at multiple centers in China The efficacy adverse events and satisfaction of the two groups were observed
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None