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NCT06915558Recruiting

Modulation of the Inflammatory Response in Bariatric Surgery

Modulation of the Inflammatory Response to Surgical Trauma: Comparison of Three Anesthetic Techniques in Bariatric Surgery Patients

Source: ClinicalTrials.gov · Last updated 8 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
90 (estimated)
First submitted
24 Mar 2025
Start date
Dec 2024
Primary completion date
Dec 2025
Lead sponsor
Hospital HM Nou Delfos
Diseases
Obesity
NCT number
NCT06915558

What you commit to

  • Study type: Observational
  • Planned participants: 90
  • From Dec 2024 to the primary completion date, Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Chronic opioid use before surgery.

Other illness

  • Severe renal or hepatic failure.
  • Uncontrolled psychiatric disorders.

Other

  • Pregnancy or breastfeeding.
  • Significant intraoperative complications requiring protocol deviation.

Who the study is looking for

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

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital HM Nou Delfos
Coordinator of this site? Confirm its status
BarcelonaSpainRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.