Status:
RECRUITING
Study of Treatment With Intensified Omeprazole Treatment to Prevent High Output Stoma 1
Lead Sponsor:
Medical University of Gdansk
Conditions:
Stoma - Ileostomy
High Output Stoma
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The goal of this clinical trial is to evaluate if intensified omeprazole therapy can reduce high-output stoma (HOS) in adults undergoing ileostomy formation surgery. The main objectives of the study a...
Detailed Description
This clinical trial investigates whether intensified omeprazole therapy can effectively reduce a condition known as high-output stoma (HOS) in adult patients undergoing ileostomy surgery. Ileostomy su...
Eligibility Criteria
Inclusion
- Adults aged 18 years or older
- Scheduled for elective or emergency surgery requiring end or loop ileostomy formation
- Able and willing to provide written informed consent
- No contraindications to omeprazole use
Exclusion
- Pregnancy or lactation
- Known hypersensitivity or allergy to proton pump inhibitors (including omeprazole)
- Conditions preventing accurate measurement of daily ileostomy output
Key Trial Info
Start Date :
April 10 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2027
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT06917963
Start Date
April 10 2025
End Date
July 1 2027
Last Update
July 31 2025
Active Locations (2)
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1
Department of Oncological, Transplant and General Surgery, Univeristy Clinical Center
Gdansk, Pomeranian Voivodeship, Poland, 80952
2
Clinical Department of Oncologic Surgery with a Subdivision of Breast, Skin, and Soft Tissue Tumor Surgery PCK Maritime Hospital
Gdynia, Poland, 81-519