Ostomy Readmission Reduction Program

Part of paid clinical trials in Los Angeles, California.

Sponsor
Cedars-Sinai Medical Center
Study ID
NCT06956274
Status
Not Yet Recruiting

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Conditions

  • Ostomy - Ileostomy or Colostomy

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Preoperative Telehealth — OTHER
    Conduct a preoperative telehealth consultation with a Certified Wound, Ostomy, and Continence Nurse (WOCN) to provide patient education on post-surgical care expectations.
  • Measure Ostomy Output — OTHER
    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.

Study Details

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.

Key Dates

Start date
May 1, 2025
Status verified
Apr 2025
Primary completion
May 1, 2026
Completion
Dec 1, 2026

Study Design

Enrollment
40 participants (estimated)

Primary Outcome Measure

Readmission to hospital within 30 Days of Surgery [ Time Frame: 30 Days Post Surgery ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Surgery Group LALos AngelesCalifornia90048-

Find similar trials in Los Angeles, CA

By research site
Surgery Group LA· Los Angeles, CA

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