Readmission and Dehydration Prevention in Patients With Elective Ileostomy

NCT06824623 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2025-06-11

No results posted yet for this study

Summary

The goal of this prospective observational study is to evaluate the adherence to DRIP score calculation and the application rate of each proposed item to prevent dehydration and readmission in patients undergoing ileostomy creation after elective colorectal resection different Italian colorectal surgical centers.

The primary endpoint is to verifythe application rate of DRIP score calculation and protocol items.

Secondary endpoints are 30, 90, and 180-day total and dehydration readmission rates.

Conditions

Sponsors & Collaborators

  • Convatec Limited

    collaborator UNKNOWN
  • Multidisciplinary Italian Study group for STOmas (MISSTO)

    lead OTHER

Principal Investigators

  • Francesco Ferrara, MD · Multidisciplinary Italian Study group for STOmas (MISSTO)

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-01
Primary Completion
2026-05-31
Completion
2026-11-30

Countries

  • Italy

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 NCT06824623 on ClinicalTrials.gov