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High-Risk For Dehydration for Dehydration

N/A
Waitlist Available
Led By Burt Cagir M FACS
Research Sponsored by The Guthrie Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days after discharge for ileostomy creation
Awards & highlights

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.

Eligible Conditions
  • Dehydration
  • Ileostomy

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days after discharge for ileostomy creation
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 days after discharge for ileostomy creation for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Readmission with 30 days
Secondary study objectives
Dehydration Events
Emergency Department Visits
Mortality
+2 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: High-Risk For DehydrationExperimental Treatment1 Intervention
Patients with an Ileostomy output of \>1L at discharge.

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Who is running the clinical trial?

The Guthrie ClinicLead Sponsor
26 Previous Clinical Trials
1,881 Total Patients Enrolled
Burt Cagir M FACSPrincipal InvestigatorRobert Packer Hospital
~0 spots leftby Sep 2025
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