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Management Of Stoma In Patients Younger Than 3 Months Old

Management of Ostomy in Neonates: A Retrospective Single-Center Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06458699
Acronym
STOMP
Enrollment
82
Registered
2024-06-14
Start date
2024-05-30
Completion date
2024-07-15
Last updated
2024-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonatal Disease, Stoma Colostomy, Stoma Ileostomy

Keywords

Ostomy, Neonate, Outcomes, Costs

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 Hirschsprung's 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.

Interventions

None listed

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Minutes to 3 Months
Healthy volunteers
No

Inclusion criteria

* Patients who had a stoma during the first 3 months of life, from January 2009 to December 2023

Exclusion criteria

* Patients who had a stoma after the first 3 months of life, from January 2009 to December 2023 * Patients without a stoma

Design outcomes

Primary

MeasureTime frameDescription
Postoperative medical complicationsthrough study completion, an average of 1 yearinfections, sepsis, dehydration, hydroelectrolytic disorders
Postoperative surgical complicationsthrough study completion, an average of 1 yeardisunion, surgical scar,

Secondary

MeasureTime frameDescription
Length of staythrough study completion, an average of 1 yeartime of hospitalization
Hospitalization coststhrough study completion, an average of 1 yearcosts by department and overall costs

Other

MeasureTime frameDescription
Redothrough study completion, an average of 1 yearNecessity to remake the stoma

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026