跳至主要内容
临床试验/2024-515183-30-00
2024-515183-30-00招募中3 期

APECS II: Comparing the efficacy of Pectoral Nerve (PECS II) Block with long-acting liposomal bupivacaine versus levobupivacaine for Mastectomy Surgery: A Multicenter Prospective Randomized Controlled Trial

St. Antonius Ziekenhuis2 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2024年6月18日最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
130
试验地点
2
主要终点
Postoperative NRS pain scores in the breast.

研究概览

简要总结

To assess whether postoperative NRS pain scores in the breast after mastectomy is lower in patients who receive a preoperative PECS II block with liposomal bupivacaine than in patients who receive a preoperative PECS II block with levobupivacaine.

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
性别
Female
接受健康志愿者

入选标准

  • Unilateral mastectomy.
  • Written informed consent according to ICH/GCP and national regulations.
  • ASA (American Society of Anesthesiologists) Class I-III.

排除标准

  • Patients < 18 year old.
  • Previous breast surgery ipsi- or contralateral (except diagnostic biopsies).
  • Not able to speak or understand the Dutch language fluently.
  • Palliative surgery.
  • Metastatic disease.
  • Pregnancy or breast feeding.
  • Psychological, neurological, familial, sociological or geographical factors that could potentially hamper compliance with the study protocol
  • Bilateral surgery.
  • Bleeding disorder or coagulopathy.
  • Chest wall deformity or infection of injection site.
  • Another (additional) nerve block (such as TPVB or epidural anesthesia).
  • Autologous or implant based breast reconstruction.
  • Known allergy for (levo)bupivacaine or local anesthetics from the amide group.
  • Known allergy or contra-indication for NSAID.
  • Chronic use of opiates preoperatively (> 12 weeks).

结局指标

主要结局

Postoperative NRS pain scores in the breast.

Postoperative NRS pain scores in the breast.

次要结局

  • Postoperative NRS pain scores in the axilla.
  • Intraoperative need of opiates (milligrams).
  • Postoperative need of opiates or other pain killers (milligrams).
  • Patient-reported chronic (> 12 weeks) pain (yes/no).
  • Patient satisfaction, measured by the BREAST-Q BCT.
  • Postoperative time that patients need to be observed in the recovery room (minutes).
  • Time until patients are discharged from the hospital (hours).
  • Use of additional anti-emetics for PONV (yes/no).
  • Vomiting (yes/no).
  • Complications (wound infection rate, hematoma, abscess, pneumothorax, local anesthesia systemic toxicity).

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

PhD candidate

Scientific

St. Antonius Ziekenhuis

研究点 (2)

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