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临床试验/NCT05590559
NCT05590559招募中不适用

Ultrasound-guided Erector Spinae Plane Block Versus Paravertebral Block in Breast Cancer Patients Undergoing Mastectomy With Immediate Reconstruction - a Non-inferiority Trial. A Single-centre Randomized Controlled Non-inferiority Trial With a Parallel Group Design

The Netherlands Cancer Institute1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
1
主要终点
Mean difference of highest numerical rating score (NRS - a linear 11 point scale for self-reported pain) during admission in the recovery room

研究概览

简要总结

The objective of this study is to assess the non-inferiority of analgesic efficacy of ESP vs PVB for patients undergoing unilateral mastectomy followed by immediate reconstruction.

详细描述

n breast cancer treatment, surgery plays a central role in combination with chemotherapy, radiation and immunotherapy. Surgery may vary from conservative breast sparing interventions to large radical mastectomies with axillary lymph node dissection that require reconstructive (prosthetic) surgery. In many instances, reconstruction is not performed immediately, but immediate reconstruction is possible and offers many advantages to patients.

The Antoni van Leeuwenhoek hospital performs a large proportion (77%) of mastectomies with immediate reconstruction in the Netherlands. The combination of mastectomy with immediate reconstruction in one operation offers an extra challenge with regards to pain control. Post-operative pain is often treated with opioids, which has systemic side effects (nausea and vomiting). Opioids also inhibit cell-mediated immunity, which is a principal defense against cancer. Regional anesthetic techniques are often performed to reduce opioid consumption and enhance postoperative recovery. The current standard for regional anesthesia for breast surgery is the paravertebral block (PVB). This technique has the potential for severe complications such as epidural hematoma, hemo- or pneumothorax. The erector spinae plane block (ESP) was first described in 2016 as a novel regional anesthetic technique for acute and chronic thoracic pain. The site of injection is distant from the pleura, major blood vessels, and spinal cord; hence, the ESP block has relatively few contraindications and has therefore been suggested as an alternative to PVB when contra-indications, such as a bleeding diathesis, are present.Multiple studies have shown a decrease in opioid consumption in patients undergoing mastectomy, when ESP was compared to placebo. ESP has also been shown to be non-inferior to PVB for pain relief in patients undergoing thoracotomy. To date, only two studies have compared ESP to PVB for breast surgery, with conflicting results. In this study, we would like to investigate whether ESP can be considered non-inferior to PVB with regards to pain relief and use of opioids.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Adult patients (18 years of age or older)
  • ASA I-III
  • Patients scheduled for elective unilateral mastectomy followed by direct reconstruction
  • Ability to give written and oral informed consent

排除标准

  • Patient refusal
  • Non-elective surgery
  • Any contraindication to paravertebral block (including bleeding diathesis, coagulopathy, severe pulmonary disease )
  • Allergy to amide-linked local anesthetics
  • Cardiac conductivity disorders (e:g: 2nd and 3rd AV-block)
  • Severe spinal malformations or history of extensive spine surgery - A history of spinal cord injury
  • Known psychiatric disorder
  • Chronic pain patients or patients already using opioids pre-operatively
  • Infection of the skin at the site of needle puncture area - Inability to give oral and written informed consent

研究组 & 干预措施

paravertebral block

Active Comparator

干预措施: Morphine (Drug)

Ultrasound-guided erector spinae plane block

Experimental

干预措施: Ultrasound-guided erector spinae plane block (Other)

结局指标

主要结局

Mean difference of highest numerical rating score (NRS - a linear 11 point scale for self-reported pain) during admission in the recovery room

时间窗: 1 day

Difference in the ratio of the means of cumulative opioid dose (administered during admission in the recovery room)

时间窗: 1 day

次要结局

  • Total opioid dose administered on day 0 and on day 1 (iv, subcutaneous or oral - converted to morphine equivalent dose (MEQ)(1 day after dose administration)
  • Complications of block (such as block failure, epidural hematoma, hemo- or pneumothorax and symptoms of toxicity of local anesthetics)(1 day)
  • Success rate as defined by satisfactory spread of local anaesthetic agents on ultrasound(1 month)
  • Patient satisfaction on a scale of 0 (extremely unsatisfied) tot 10 (extremely satisfied)(1 month)
  • Ease of procedure (self-reported by anaesthetist on scale of 1-5)(1 month)
  • Highest pain score on day 0 and 1(1 day)
  • Time to readiness for discharge from the recovery room(1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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