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Study identifier: NCT07354750 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Parasternal Plane Block on Intraoperative Nociception

Condition: Median Sternotomy · Pain Management  ·  Sponsor: Diskapi Yildirim Beyazit Education and Research Hospital

PhaseNA
Planned participants60
Who can joinAll sexes, 6 Months to 7 Years
Healthy volunteersNo

About this study

Effective pain control during pediatric cardiac surgery remains a major clinical challenge, particularly in procedures involving median sternotomy, which is associated with intense nociceptive stimulation. Inadequate intraoperative analgesia may lead to increased opioid requirements, hemodynamic instability, delayed extubation, and prolonged intensive care unit stay. Objective monitoring of nociception may provide valuable information beyond conventional hemodynamic parameters in this vulnerable population. This prospective randomized controlled study aims to evaluate the effect of ultrasound-guided parasternal plane block on intraoperative nociception in pediatric patients undergoing cardiac surgery with median sternotomy. Intraoperative nociception will be objectively assessed using the Pain Index Monitor (PAM), based on skin conductance measurements. The results of this study are expected to provide objective evidence regarding the efficacy of parasternal plane block in attenuating nociceptive responses during pediatric cardiac surgery and to support the integration of regional anesthesia techniques and objective nociception monitoring into perioperative pain management strategies for children.

This description comes directly from the study's public registry record.

Talk to the study team

Elif Şule Özdemir Sezgi  ·  00905059209638  ·  elifsule-91@hotmail.com

Aslı Dönmez  ·  00905322256473  ·  aslidonmez@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Ankara Etlik City HospitalAnkara, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07354750