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临床试验/NCT04336917
NCT04336917已完成4 期

Ultrasound Guided Rhomboid Intercostal and Subserratus Plane Block in Breast Cancer Surgeries

Konya Meram State Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2020年8月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
50
试验地点
1
主要终点
Postoperative opiod consumption

研究概览

简要总结

Postoperative analgesia after breast cancer surgery is a challenge for anesthesiologists due to the complex innervation of the breast. Interfascial plane blocks of the chest are gaining widespread popularity with the introduction of ultrasonography into the regional anesthesia practice. We aimed to investigate the efficacy of Rhomboid intercostal and subserratus plane block (RISS) for postoperative analgesia in patients undergoing breast cancer surgery.

详细描述

This prospective randomized controlled trial will be carried out on female patients who scheduled for breast cancer surgery. Our hypotesis is that this new interfascial plane block technique will able to provide postoperative analgesia in breast cancer surgery.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients aged 18-85 years and ASA physiological score I-III who undergone breast cancer surgery

排除标准

  • Patients refused to participate.
  • Patients with known or suspected allergy to the used medication.
  • Patients with psychiatric-neurological disorders that may affect pain perception,
  • Patients regularly taking antipsychotics and antidepressants.
  • Patients with potential risk of coagulopathy.
  • Uncooperative patients.

研究组 & 干预措施

Group Rhomboid Intercostal and Subserratus Plane Block

Active Comparator

In addition to routine standard perioperative and postoperative analgesic protocol participants will recieve Rhomboid Intercostal and Subserratus Plane Block under ultrasound guidence at the end of the surgery.

干预措施: Rhomboid Intercostal and Subserratus Plane Block with local anesthetic (Drug)

结局指标

主要结局

Postoperative opiod consumption

时间窗: The first 24 hours postoperatively

Opioid consumptions for both group will be recorded.

次要结局

  • Postoperative pain scores(The first 24 hours postoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Betul Kozanhan

Ass.Prof.

Konya Meram State Hospital

研究点 (1)

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