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NCT06824623: PREDESTO

Readmission and Dehydration Prevention in Patients With Elective Ileostomy

Recruiting now Last updated 11 June 2025
What this trial tests

trial in Ileostomy - Stoma in 300 participants. Currently enrolling.

Timeline
1 June 2025
Primary endpoint
31 May 2026
30 November 2026

Quick facts

Lead sponsorMultidisciplinary Italian Study group for STOmas (MISSTO)
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment300
Start date1 June 2025
Primary completion31 May 2026
Estimated completion30 November 2026
Sites7 locations across Italy

Conditions studied

Sponsor

Multidisciplinary Italian Study group for STOmas (MISSTO)

Who can join

18 and older, any sex, with Ileostomy - Stoma or Colorectal Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Ileostomy - Stoma

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06824623.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing