About this trial
This prospective observational study aims to compare three routinely used postoperative analgesia techniques in patients undergoing open heart surgery: intravenous analgesia, thoracic epidural analgesia (TEA), and bilateral erector spinae plane block (ESPB). The primary objective is to evaluate the impact of these analgesia modalities on the development of chronic postoperative pain at 3 months. Secondary objectives include assessing postoperative acute pain scores, additional analgesic requirements, extubation time, mobilization time, intensive care unit stay, hospital stay, respiratory complications, and the relationship between acute and chronic pain. No intervention is assigned by protocol, and all analgesia methods are applied as part of routine clinical practice.
Eligibility criteria
Qualifiers
Adults aged 18 to 85 years
Classified as ASA physical status I-III
Scheduled to undergo open heart surgery with median sternotomy
BMI < 35 kg/m²
Disqualifiers
Age < 18 or > 85 years
BMI ≥ 35 kg/m²
Coagulation disorders
Infection at the intervention site
Trial design
Treatments tested in this trial
- Intravenous Analgesia
- Thoracic Epidural Analgesia (TEA)
- Erector Spinae Plane Block (ESPB)