← Eichor
Study identifier: NCT06824623 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Readmission and Dehydration Prevention in Patients With Elective Ileostomy

Condition: Ileostomy - Stoma · Colorectal Surgery · Dehydration  ·  Sponsor: Multidisciplinary Italian Study group for STOmas (MISSTO)

PhaseN/A
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Francesco Ferrara, MD  ·  +393343035829  ·  frr.fra@gmail.com

Dario Parini, MD  ·  +393295477268  ·  dario.parini@gmail.com

Always discuss trial participation with your own doctor first.

Locations (7)

ASST Ovest Milanese, Ospedale di LegnanoLegnano, Italy, ItalyRecruiting
Luigi Sacco University HospitalMilan, Italy, ItalyRecruiting
Università degli Studi Milano-Bicocca, Ospedale San GerardoMonza, Italy, ItalyRecruiting
University of Palermo, "Paolo Giaccone" University HospitalPalermo, Italy, ItalyRecruiting
Ospedale Santa Maria della MisericordiaRovigo, Italy, ItalyRecruiting
ASST Nord Milano, Ospedale Città di Sesto San GiovanniSesto San Giovanni, Italy, ItalyRecruiting
IRCCS Policlinico di BolognaBologna, ItalyRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06824623