Paravertebral Block for Postoperative Analgesia in Children Undergoing Lateral Incision Cardiac Surgery With CBP - Trial NCT06312904
Access comprehensive clinical trial information for NCT06312904 through Pure Global AI's free database. This phase not specified trial is sponsored by Chinese Academy of Medical Sciences, Fuwai Hospital and is currently Not yet recruiting. The study focuses on Postoperative Pain. Target enrollment is 100 participants.
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Study Focus
Sponsor & Location
Chinese Academy of Medical Sciences, Fuwai Hospital
Timeline & Enrollment
N/A
Mar 11, 2024
Dec 30, 2024
Primary Outcome
opioid consumption during the first 24h after surgery
Summary
This study aims to compare the effect of paravertebral block and local infiltration
 anesthesia on postoperative analgesia in children undergoing lateral incision cardiac surgery
 with cardiopulmonary bypass. The researchers hope to investigate whether children who undergo
 paravertebral block experience less postoperative pain, have fewer postoperative
 complications, and recover more quickly.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06312904
Non-Device Trial

