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Ostomy Readmission Reduction Program

Ostomy Readmission Reduction Program

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06956274
Enrollment
40
Registered
2025-05-04
Start date
2025-05-01
Completion date
2026-12-01
Last updated
2025-05-04

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

Conditions

Ostomy - Ileostomy or Colostomy

Brief summary

The purpose of this study is to reduce complications like peristomal skin issues, stoma-related problems, dehydration, and other preventable factors that can lead to re-hospitalization within the first 30 days after surgery.

Interventions

OTHERPreoperative Telehealth

Conduct a preoperative telehealth consultation with a Certified Wound, Ostomy, and Continence Nurse (WOCN) to provide patient education on post-surgical care expectations.

OTHERMeasure Ostomy Output

Patients will be sent home with a measuring container (graduated container) and will measure their ostomy output every 12 hours and record it in a pad that will be provided to them.

Sponsors

Cedars-Sinai Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Elective operations involving an ileostomy or a colostomy * Individuals 18 years old or older are included

Exclusion criteria

* Individuals under age 18 * Pregnant patients * Emergency operations * Patients with existing pre operative ostomies

Design outcomes

Primary

MeasureTime frameDescription
Readmission to hospital within 30 Days of Surgery30 Days Post SurgeryThe proportion of participants who are readmitted to the hospital within 30 days following surgery. Readmissions will be evaluated for any reason, including complications, adverse events, or recovery issues that necessitate hospitalization after the initial surgical procedure.

Secondary

MeasureTime frameDescription
Hospital Length of StayFrom index surgery to discharge (up to 30 days postoperatively)Total duration of hospitalization from the time of the index surgery until discharge.
Incidence of Acute Kidney Injury (AKI)From index surgery through 30 days postoperativelyNumber of participants who develop AKI, defined as an increase in serum creatinine of ≥0.3 mg/dL from baseline, during index admission or upon 30-day readmission.
Incidence of Peristomal Skin ComplicationsFrom index surgery through 30 days postoperativelyNumber of participants who develop peristomal skin problems (e.g., irritation, excoriation, or dermatitis) during the index admission or within 30 days postoperatively.
Incidence of Stoma-Related LeakageFrom index surgery through 30 days postoperativelyNumber of participants who experience unintended escape of stoma output (leakage) during index admission or within 30 days postoperatively.

Countries

United States

Contacts

Primary ContactYosef Nasseri, MD
Yosef.Nasseri@cshs.org310-289-1518

Outcome results

None listed

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