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临床试验/CTIS2024-513301-30-00
CTIS2024-513301-30-00进行中(未招募)1 期

Evaluation of the effect of para-sternal block on postoperative respiratory function after sternotomy cardiac surgery.Prospective, controlled, randomized, single-blind study with independent assessment of outcome

Centre Hospitalier Universitaire Amiens Picardie0 个研究点目标入组 84 人开始时间: 2024年4月5日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
84

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

年龄范围
18 至 64(—)
性别
All

入选标准

  • Patients over 18 years of age, Elective cardiac surgery under CEC with sternotomy (valve replacement, coronary artery bypass graft or combined combined surgery with valve replacement and coronary bypass surgery), Patient's written informed consent

排除标准

  • Thoracotomy approach, Autoimmune disorder, Transplant recipient, Inclusion in another study within the last 30 days, Pregnancy, Women of childbearing age should have a negative urine HCG pregnancy test, Mini-sternotomy approach, Opioid dependence or chronic medication opioid medication, Chronic use of benzodiazepines (respiratory depressant or respiratory depressant or may affect respiratory function respiratory function), Contraindication or allergy to local anesthetics, Emergency surgery, Acute infectious endocarditis, Immunosuppressive treatment or steroids (prednisone > 0.5mg/kg/day or equivalent), AIDS with CD4 count <200/mm3

研究者

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