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Recruiting Phase 4 NCT06812832

NCT06812832 Simethicone as Part of ERAS in Bariatric Surgery Patients

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Clinical Trial Summary
NCT ID NCT06812832
Status Recruiting
Phase Phase 4
Sponsor Madigan Army Medical Center
Condition Simethicone
Study Type INTERVENTIONAL
Enrollment 260 participants
Start Date 2025-04-08
Primary Completion 2028-03

Trial Parameters

Condition Simethicone
Sponsor Madigan Army Medical Center
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 260
Sex ALL
Min Age 18 Years
Max Age 89 Years
Start Date 2025-04-08
Completion 2028-03
Interventions
Simethicone 80 MGPlacebo

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Brief Summary

By conducting this study, we hope to assess if simethicone (also known as Gas Relief or GasX) has an effect on improving gas pain and bloating specifically in patients undergoing foregut procedures to include bariatric procedures (sleeve gastrectomy, Roux-en-Y gastric bypass), hiatal hernia, and gastric surgery. The purpose of this research is to gather information on the safety and effectiveness of simethicone. Simethicone (more commonly known as Gas Relief or Gas-X) relieves pressure, bloating, and fullness commonly referred to as gas. It is FDA approved. The use of this medication in this research study is consistent with labeling indications.

Eligibility Criteria

Inclusion Criteria: * Foregut procedures Exclusion Criteria: * Non-foregut procedures * Allergy to simethicone * Pregnancy or breastfeeding * Minors under 18 years of age

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