Viewing Study NCT06458699



Ignite Creation Date: 2024-06-16 @ 11:52 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06458699
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-06-14
First Post: 2024-06-05

Brief Title: Management Of Stoma In Patients Younger Than 3 Months Old
Sponsor: University Hospital Clermont-Ferrand
Organization: University Hospital Clermont-Ferrand

Study Overview

Official Title: Management of Ostomy in Neonates A Retrospective Single-Center Study
Status: ACTIVE_NOT_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: STOMP
Brief Summary: Indications for jejunostomy ileostomy or colostomy vary in the neonatal population The most common etiologies are congenital anomalies such as anorectal malformations intestinal atresia or Hirschsprungs disease but also acquired conditions such as enterocolitis or intestinal perforation The aim of these stomas is to divert stool in the event of intestinal obstruction or risk of fecal contamination

Depending on the indication and the type of stoma used the post-operative follow-up such as resumption of intestinal transit and feeding secondary closure of the stoma or not and the duration and cost of hospitalization differ

The aim of this study is to compare these differences in order to extract an optimal management strategy in the light of what is reported in the international scientific literature
Detailed Description: The investigators gathered the data of patients born between January 2009 and December 2023 who had an ostomy made during the first three months of their life

The investigators then analyzed the patients outcomes postoperative complications length of stay cost of hospitalization depending on the etiology of their primary disease

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