About this trial
Analgesic management in thoracic surgery presents a particular challenge for the anesthesiologist, given the intensity of postoperative pain associated with thoracotomy, a surgical procedure that can impact respiratory function and the patient's subsequent recovery. Epidural analgesia is the gold standard. When epidural catheter placement is not feasible, erector spinae plane block is a safe alternative. The ultrasound target is easily visualized, and the injection site is far from the neuraxis, pleura, and major vascular structures. Consequently, this block has been incorporated into standard clinical practice as a treatment option for patients with complex cases or as an alternative approach when epidural catheter placement is not feasible. The primary objective of this study is to assess the effectiveness of postoperative analgesia in patients undergoing elective thoracic surgery.
Study Population Design A prospective observational follow-up study will be conducted. ASA I-III patients undergoing scheduled thoracic surgery between November 1 and December 31, 2025, will be included. Their analgesic management will be based on standard clinical practice.
Eligibility criteria
Qualifiers
Patients undergoing thoracic surgery between July 1 and October 31, 2020.
Age over 18.
ASA I-III.
Signed informed consent
Disqualifiers
ASA IV-V.
Chronic opioid treatment or treatment in the Chronic Pain Unit.
Intravenous drug abuse.
Local anesthetic allergy.
Trial design
Treatments tested in this trial
- Postoperative pain through Visual analogue scale
- Postoperative complications