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临床试验/NCT04506762
NCT04506762终止不适用

Does Bilateral Continuous Peri Operative Erector Spinae Plane Block Improve The Enhanced Recovery Program After Open Heart Surgeries in Adults?

Vinmec Healthcare System1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2020年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
20
试验地点
1
主要终点
Length of post operative stay in Hospital

研究概览

简要总结

To demonstrate if the addition of peri-operative regional analgesia by Bilateral ESP catheters improves the enhanced recovery program after open heart surgeries for the duration of hospitalisation, quality of analgesia, Consumption of peri-operative opioids, quality of recovery and quality of life.

Patients will be randomly divided in 2 groups Group 1 With the actual standards of care for enhanced recovery after cardiac surgery including opioid sparing peri operative analgesia Group 2 With the actual standards of care for enhanced recovery after cardiac surgery replacing the opioid analgesia by a peri operative analgesia by bilateral ESP catheters

详细描述

I. CONSULTING PHASE: 1 WEEK BEFORE SURGERY

  1. Preoperative information, education and counselling: patient and families receive dedicated preoperative counselling including information packets.
  2. Preoperative optimization: medical optimization before surgery, including renal, pulmonary, and endocrine function.
  3. Smoking and alcohol cessation: smoking and alcohol cessation advised and promoted before surgery.
  4. Preoperative nutrition status: patients screened for nutritional status and counselling given for a protein-rich diet at least the week before the surgery.

II. PREOPERATIVE PHASE: 2 DAYS BEFORE SURGERY

  1. Preoperative fasting and carbohydrate treatment: patients are kept NPO 8h before surgery except for oral carbohydrate beverage given 2-4h before surgery.
  2. Reviewed all examination results: cardiac echography, X-ray, biology's tests
  3. Consents signed.
  4. Authorization operative be signed
  5. Preoperative multimodal analgesic initiated : before surgery 2 h Gabapentin: 600 mg (P.O) Acetaminophen: 500 mg (P.O) Hydroxyzine: 50 mg (P.O)

III. INTRAOPERATIVE PHASE:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Open heart surgeries: Valvulopathies ( 1-2 valves, repair or replacement)
  • Congenital heart disease (Risk Adjustment in Congenital Heart Surgery Category 1-2 ( VSD, ASD, T4F)
  • Fraction ejection > 50%,
  • PAPS < 50 mmHg.
  • Age from 18-60 years old.
  • Consent participation

排除标准

  • Refusal participation.
  • Allergy to LA
  • Severe thoracic Scoliosis
  • Valvulopathies association with :
  • BENTALL procedure
  • Deficit mental
  • Alcoholics,
  • Heroine addicted
  • Insufficient renal
  • liver failure
  • Endocarditis <1 year
  • Stroke <3 months
  • MI <3 months
  • Bloc AV II or III with Pacemaker permanent

结局指标

主要结局

Length of post operative stay in Hospital

时间窗: 10 days

Duration of hospitalisation

次要结局

  • Length of post operative stay in Intensive care unit(3 days)
  • Time to 1st mobilisation(3 days)
  • Quality of recovery(1 month)

研究者

发起方
Vinmec Healthcare System
申办方类型
Other
责任方
Principal Investigator
主要研究者

Philippe Macaire

MD

Vinmec Healthcare System

研究点 (1)

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