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临床试验/NCT06413290
NCT06413290
已完成
不适用

Doppler Evaluation of Ultrasound-guided Pectointercostal Fascial Plane Block in Cardiac Surgery

Antalya Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 40 人2024年5月15日

概览

阶段
不适用
干预措施
PIFP block group
疾病 / 适应症
Cardiovascular Surgery
发起方
Antalya Training and Research Hospital
入组人数
40
试验地点
1
主要终点
blood volume
状态
已完成
最后更新
3个月前

概览

简要总结

The aim of this study was to evaluate the effect of pectointercostal fascial plane block on regional haemodynamic parameters in patients undergoing cardiac surgery.

详细描述

Perioperative pain management has become an important component of Enhanced Recovery After Surgery (ERAS) protocols in patients undergoing cardiac surgery. Pain is most intense in the first two days after cardiac surgery. Inadequate pain control has been shown to cause an increase in pulmonary complications due to inadequate mobility and coughing, an increase in sympathetic activation, an increase in myocardial infarction and thromboembolic events, delayed wound healing, and prolonged hospital and intensive care unit stay. Non-steroidal anti-inflammatory drugs (NSAIDs), paracetamol, opioids, epidural anesthesia and ultrasound-guided fascial plane blocks are widely used for pain management after cardiac surgery. The pectointercostal fascial plane (PIFP) block is an ultrasound-guided, superficial fascial plane block that can be applied as part of multimodal postoperative analgesia, especially after cardiac surgery. PIFB block has been shown to reduce postoperative analgesic consumption and improve pain scores not only in patients undergoing cardiac surgery but also in non-cardiac surgeries and thoracic procedures. The aim of this study was to evaluate the effect of PIFP block on regional haemodynamic parameters in patients undergoing cardiac surgery.

注册库
clinicaltrials.gov
开始日期
2024年5月15日
结束日期
2025年12月30日
最后更新
3个月前
研究类型
Observational
性别
All

研究者

发起方
Antalya Training and Research Hospital
责任方
Sponsor

入排标准

入选标准

  • elective cardiac surgery
  • over 18 years, adult
  • American Society of Anaesthesiology (ASA) I-III

排除标准

  • history of cerebrovascular disease
  • history of Alzheimer's disease
  • mental disorder
  • emergency surgery
  • re-operated due to surgery-related complications
  • allergy to local anaesthetics
  • declining to give written informed consent

研究组 & 干预措施

PIFP block group

Before the anesthesia induction, PIFP block will be performed

干预措施: PIFP block group

Control group

No intervention

干预措施: Control group

结局指标

主要结局

blood volume

时间窗: 1 hour

The regional haemodynamic impact of PIDB block will be evaluated by Doppler ultrasound

次要结局

  • postoperative opioid consumption(24 hours)
  • postoperative Numerical Rating Scale (NRS) pain scores(24 hours)
  • length of hospital stay(5 days)

研究点 (1)

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