Readmission and Dehydration Prevention in Patients With Elective Ileostomy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMultidisciplinary Italian Study group for STOmas (MISSTO)
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 protocol items.
Secondary endpoints are 30, 90, and 180-day total and dehydration readmission rates.
Eligibility criteria
Qualifiers
All patients with elective ileostomy performed during the study period for benign or malignant colorectal disease
Age > 18 years
Written consent
Disqualifiers
Emergency surgery
Other ostomy than ileostomy
Trial design
Treatments tested in this trial
- Not listed
Trial groups
300 Participants
are grouped into 1 trial groupSponsors and collaborators
Multidisciplinary Italian Study group for STOmas (MISSTO)
Lead sponsor
Convatec Limited
Collaborator
Source ClinicalTrials.gov