Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
40 participants
OBSERVATIONAL
2025-05-01
2026-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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Preoperative Telehealth
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
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.
Eligibility Criteria
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Inclusion Criteria
* Individuals 18 years old or older are included
Exclusion Criteria
* Pregnant patients
* Emergency operations
* Patients with existing pre operative ostomies
18 Years
ALL
No
Sponsors
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Cedars-Sinai Medical Center
OTHER
Responsible Party
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Yosef Nasseri, MD
Colon and Rectal Surgeon
Principal Investigators
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Yosef Nasseri, MD
Role: PRINCIPAL_INVESTIGATOR
Cedars-Sinai Medical Center
Locations
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Surgery Group LA
Los Angeles, California, United States
Countries
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Central Contacts
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Other Identifiers
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STUDY00003920
Identifier Type: -
Identifier Source: org_study_id
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