MedTrace Logo

Evaluating Ileostomy Hydration Protocol

NCT04669964 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2023-02-21

No results posted yet for this study

Summary

This is a prospective observational study on patients who undergo an ileostomy creation after implementing a hydration algorithm as routine care at Robert Packer Hospital. The Department of Surgery will be implementing a protocol to prevent dehydration for patients with high output ileostomies. Patients with high output ileostomies are at an increased risk for readmission for dehydration. By reviewing the data after applying this standardized hydration protocol, we can assess its efficacy on readmission rates and comorbidities stemming from dehydration.

Conditions

  • Ileostomy - Stoma
  • Ileostomy; Complications
  • Dehydration

Interventions

PROCEDURE

Intravenous Hydration

Patients will receive daily intravenous hydration of normal saline based on their ileostomy output.

Sponsors & Collaborators

  • The Guthrie Clinic

    lead OTHER

Principal Investigators

  • Burt Cagir M FACS · Robert Packer Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2024-01-01
Completion
2025-01-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04669964 on ClinicalTrials.gov