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Video-assisted thoracoscopic surgery (VATS) is a minimally invasive procedure performed through small thoracic incisions, but postoperative pain remains significant due to tissue and rib trauma. Poorly controlled pain may lead to chronic postoperative pain; therefore, optimal analgesia is essential.
According to PROSPECT guidelines, erector spinae plane block (ESPB) or paravertebral block (PVB) are recommended for VATS. The recently defined serratus posterior superior intercostal plane block (SPSIPB) provides analgesia between C3-T10 levels, but its efficacy compared with ESPB has not been studied.
This study aims to compare postoperative analgesic efficacy and patient satisfaction between ESPB and SPSIPB in VATS patients.
Full description
Video-assisted thoracoscopic surgery (VATS) is a minimally invasive procedure performed through small thoracic incisions, but postoperative pain remains significant due to tissue and rib trauma. Poorly controlled pain may lead to chronic postoperative pain; therefore, optimal analgesia is essential.
According to PROSPECT guidelines, erector spinae plane block (ESPB) or paravertebral block (PVB) are recommended for VATS. The recently defined serratus posterior superior intercostal plane block (SPSIPB) provides analgesia between C3-T10 levels, but its efficacy compared with ESPB has not been studied.
This study aims to compare postoperative analgesic efficacy and patient satisfaction between ESPB and SPSIPB in VATS patients.
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Inclusion criteria
Exclusion criteria
Patients with coagulopathy
Patients with a history of local anesthetic allergy or toxicity
Patients with hepatic or renal failure
Patients with uncontrolled diabetes
Patients with uncontrolled hypertension
Mentally disabled patients
Patients receiving chronic pain treatment (opioid users)
Patients using antidepressant medication
Patients with neuropathic pain
Mentally disabled patients
Presence of infection at the injection site
Pregnant or breastfeeding women, or those with suspected pregnancy
Primary purpose
Allocation
Interventional model
Masking
90 participants in 2 patient groups
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Central trial contact
Eralp Çevikkalp; Emre ULUSOY
Data sourced from clinicaltrials.gov
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