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The goal of this clinical trial is to determine which regional block provides superior analgesia in pediatric patients undergoing thoracic surgery. The main questions it aims to answer are: * Does one block technique provide better pain relief? * Does the choice of block reduce opioid requirements and complication rates? Researchers will compare two block techniques to see if one offers an effective opioid-sparing strategy that improves patient comfort and reduces side effects. Participants will: * Receive one of the studied block interventions during thoracic surgery. * Be monitored for postoperative pain scores, opioid consumption, and any complications.
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