Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT06915558

Modulation of the Inflammatory Response in Bariatric Surgery

Led by Hospital HM Nou Delfos · Updated on 2025-04-08

90

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will evaluate how different anesthesia techniques affect inflammation after bariatric surgery. Patients will be randomly assigned to receive one of three approaches: opioid-free anesthesia, intravenous anesthesia with opioids, or inhalational anesthesia with opioids. The study will measure blood levels of inflammation-related substances (such as IL-6, CRP, cortisol, ESR , WBC and lactate) at several time points before and after surgery. Heart rate variability will also be monitored as an indicator of the body's stress response. The results may help identify anesthesia strategies that reduce inflammation and improve recovery in patients undergoing bariatric surgery.

CONDITIONS

Official Title

Modulation of the Inflammatory Response in Bariatric Surgery

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for bariatric surgery.
  • Age 18-65 years.
  • BMI 63 30 kg/m�B2.
  • ASA physical status II-III.
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding.
  • Chronic opioid use before surgery.
  • Severe renal or hepatic failure.
  • Uncontrolled psychiatric disorders.
  • Significant intraoperative complications requiring protocol deviation.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital HM Nou Delfos

Barcelona, Barcelona, Spain, 08023

Actively Recruiting

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Research Team

H

Hipolito Labandeyra Gonzalez, Anesthesiologist

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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