Readmission and Dehydration Prevention in Patients With Elective Ileostomy
Recruiting
Observational Study
Ileostomy - Stoma
Colorectal Surgery
Dehydration
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 300 (estimated)
- Sponsor
- Multidisciplinary Italian Study group for STOmas (MISSTO) · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All patients with elective ileostomy performed during the study period for benign or malignant colorectal disease
* Age \> 18 years
* Written consent
Exclusion Criteria:
* Emergency surgery
* Other ostomy than ileostomy
Contacts