跳至主要内容
临床试验/CTRI/2019/10/021591
CTRI/2019/10/021591尚未招募未知

â??Ultrasound guided Bilateral Pecto-intercostal Fascial Block: Role as a preemptive analgesic adjunct in fast tracking for mitigating postoperative Sternotomy Pain.â??

Shree Chitra Tirunal Institute for Medical Sciences and Technology0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Inclusion criteria
  • Adult patients coming for elective cardiac
  • surgery having CAD for CABG.
  • > 40 years old and < 75 years old
  • Median sternotomy
  • Patient undergoing Coronary Artery bypass

排除标准

  • Emergency Surgeries.
  • Redo-surgeries.
  • Open Sternum
  • Left Ventricular Ejection Fraction < 35%
  • Preoperative use of narcotics or illicit drug
  • History of chronic intractable non-cardiac pain.
  • Liver or Kidney disease
  • Allergy to Amide group of anaesthetics, Morphine
  • or Fentanyl.
  • Arrhythmia history or rhythm disturbances
  • documented in ECG.
  • Haemodynamically unstable patients, already on
  • preoperative inotropic support or Intraarterial
  • balloon pumps(IABP).
  • Anticipated surgery or Surgery lasting more than
  • Patient on ventilator time more than 12hrs or
  • planned for overnight ventilation.
  • Patients refusing to participate.
  • Patients refusing for parting with medical data
  • for analysis.
  • Patients refusing to participate after the start
  • of study and desire to leave the study at any
  • point of time.
  • Patients currently enrolled in another study.
  • Patients with inability to provide informed
  • written consent.
  • Inability to complete Pain assessments.
  • Post-operative complications with underlying
  • cardio-respiratory cause requiring return to
  • operative room for re-explorations or
  • reinstitution of mechanical ventilation.
  • Patients refusing the offered therapeutic
  • options in either group.
  • No bias against gender, class, caste, ethnicity,
  • race and will be considered as inclusion or
  • exclusion criteria.

研究者

发起方
Shree Chitra Tirunal Institute for Medical Sciences and Technology

相似试验