RecruitingN/AOther

Modulation of the Inflammatory Response in Bariatric Surgery

Sponsored by Hospital HM Nou Delfos

NCT ID
NCT06915558
Target Enrollment
90 participants
Start Date
2024-12-02
Est. Completion
2025-12-02

About This Study

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 Studied

ObesityBariatric Surgery CandidateInflammationPostoperative PainOpioid-Free AnesthesiaHeart Rate Variability

Interventions

  • Opioid-Free Anesthesia (OFA)
  • Opioid-Based Intravenous Anesthesia (OBA-IV)
  • Opioid-Based Inhalational Anesthesia (OBA-Inh)

Eligibility

Age:18 Years - 65 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Patients scheduled for bariatric surgery.
* Age 18-65 years.
* BMI ≥ 30 kg/m².
* ASA physical status II-III.

Exclusion Criteria:

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

Study Locations (1)

Hospital HM Nou Delfos
Barcelona, Barcelona, Spain

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Hipolito Labandeyra Gonzalez, Anesthesiologist
CONTACT
+34696055181hipolitolabandeyra@gmail.com
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source

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