Readmission and Dehydration Prevention in Patients With Elective Ileostomy
Recruiting now
Conditions studied: Ileostomy - Stoma, Colorectal Surgery, Dehydration
In brief
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.
Key facts
- Study ID
- NCT06824623
- Run by
- Multidisciplinary Italian Study group for STOmas (MISSTO)
- People needed
- 300
- Starts
- 2025-06-01
- Expected to finish
- 2026-11-30
- Last updated by the study team
- 2025-06-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients with elective ileostomy performed during the study period for benign or malignant colorectal disease
- Age > 18 years
- Written consent
You may not qualify if…
- Emergency surgery
- Other ostomy than ileostomy
Where it is running
- ASST Ovest Milanese, Ospedale di Legnano — Legnano, Italy, Italy (enrolling)
- Luigi Sacco University Hospital — Milan, Italy, Italy (enrolling)
- Università degli Studi Milano-Bicocca, Ospedale San Gerardo — Monza, Italy, Italy (enrolling)
- University of Palermo, "Paolo Giaccone" University Hospital — Palermo, Italy, Italy (enrolling)
- Ospedale Santa Maria della Misericordia — Rovigo, Italy, Italy (enrolling)
- ASST Nord Milano, Ospedale Città di Sesto San Giovanni — Sesto San Giovanni, Italy, Italy (enrolling)
- IRCCS Policlinico di Bologna — Bologna, Italy (enrolling)
Full record on ClinicalTrials.gov
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