Viewing Study NCT06517407



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06517407
Status: RECRUITING
Last Update Posted: None
First Post: 2024-07-08

Brief Title: Para Versus Trans Rectus Stoma Placement for Prevention of Stoma Related Complications
Sponsor: None
Organization: None

Study Overview

Official Title: Para Rectus Versus Trans Rectus Stoma Placement for Prevention of Stoma Related Complications
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Fecal divertion is a surgical procedure by which stoma is constructed through exteriorization of small intestine or large intestineloop or end stomaThere are many indications for enterostomies such as malignancy bleeding per rectum MVO Volvulus iatrogenic colon injury adhesive bands etc

Many factors concerning the operative technique are considered to influence the incidence of stoma related complications such as stoma prolapse retraction stenosis para stomal herniation para stomal soiling oedema and ileus Site of stoma creation in relation to rectus abdominis muscle is believed to be one of them
Detailed Description: Fecal divertion is a surgical procedure by which stoma is constructed through exteriorization of small intestine or large intestineloop or end stomaThere are many indications for enterostomies such as malignancy bleeding per rectum MVO Volvulus iatrogenic colon injury adhesive bands

Many factors concerning the operative technique are considered to influence the incidence of stoma related complications such as stoma prolapse retraction stenosis para stomal herniation para stomal soiling oedema and ileus Site of stoma creation in relation to rectus abdominis muscle is believed to be one of them

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