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临床试验/NCT04106999
NCT04106999尚未招募2 期

Dexmedetomidine and Inflammation in HIPEC Cases: A Case Series

University of British Columbia1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
20
试验地点
1
主要终点
Inflammation

研究概览

简要总结

Inflammation is associated with an increased risk of cancer recurrence. Various methods have been used to decrease the inflammatory response induced by the cancer and surgery. In this study the investigators would like determine if a commonly used sedative drug (dexmedtomidine) has an impact on this inflammatory state when used as part of the anesthetic. The investigators will conduct a pilot study with 20 patients undergoing a Hyperthermic Intraperitoneal Chemotherapy (HIPEC) procedure as part of their cancer treatment. 10 patients will receive the standard of care for anesthesia during the cancer surgery and a placebo infusion of normal saline at a rate consistent to that of the study drug. 10 additional patients will receive the same standard of care anesthetic plan with the addition of an infusion of dexmeditomidine during the procedure. The investigators will measure the degree of inflammation before, during and after the surgical procedure by looking at the levels of inflammatory markers in blood samples. The goal is to determine if the addition of dexmodtomidine affects the inflammatory state of patients undergoing a HIPEC procedure. This information will be used to guide future studies aiming at decreasing cancer recurrence and improve patient outcomes.

详细描述

Purpose: To investigate the use of intra-operative dexmedetomidine infusions to reduce the inflammatory and stress response of cytoreductive treatment and hyperthermic intra-peritoneal chemotherapy (HIPEC).

Hypothesis: HIPEC surgery patients who receive an intra-operative infusion of dexmedetomidine in addition to the current standard of care, consisting of parenteral and enteral opioids and thoracic epidural will have a reduction in their inflammatory markers intra-operatively, in PACU, POD1 and POD5 and a reduction in oral morphine equivalent opioid consumption in PACU and POD1, in comparison to those who receive a placebo infusion.

Justification: Surgical tumor excision is a cornerstone of primary cancer treatment, but is also recognized as one of the greatest risk factors for metastatic spread. The perioperative period, characterized by the surgical stress response and pharmacologic-induced angiogenesis and immunomodulation, results in a physiologic environment that supports tumor spread and distant reimplantation. There is potential for anesthesiologists to modulate the unwanted consequences of the stress response on the immune system and minimize residual disease by altering their anesthetic plan.

Dexmedtomidine is a commonly used sedative that can be used as part of an anesthetic during surgery. In vitro and animal studies have shown that dexmedtomidine decreases the inflammatory response but no research has been conducted with cancer-related conditions.

Objective: To determine if dexmedtomidine, when used intraoperatively, can decrease the levels of inflammation in patients a Hyperthermic Intraperitoneal Chemotherapy (HIPEC) procedure as part of their cancer treatment.

研究设计

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

盲法说明

A blinded syringe with either the placebo or study drug will be given to the anesthesiologist involved in that patient's care. All other care providers will be blinded to the study group

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing a Hyperthermic Intraperitoneal Chemotherapy (HIPEC) procedure as part of their cancer treatment at Vancover General Hospital
  • 18 years of age or older
  • Able to provide informed consent
  • Expected stay 5 days or greater in hospital
  • Presenting for HIPEC with Colon or Appendix Cancer

排除标准

  • Contraindication to dexmedtomidine use including allergy or sensitivity to the drug
  • Pregnancy
  • ASA greater than or equal to 4
  • Significant liver disease
  • Current use of steroid or immunosuppressive medication
  • Mesothelioma tumour origin
  • Current use of clonidine
  • Current opioid use exceeding 30mg of oral morphine equivalents
  • Patient not eligible or patient refusal to have a thoracic epidural

研究组 & 干预措施

Placebo

Placebo Comparator

Normal Saline will be infused as per the protocol

干预措施: Placebos (Drug)

Intervention group

Experimental

Dexmedetomidine will be infused as per the protocol

干预措施: Dexmedetomidine (Drug)

结局指标

主要结局

Inflammation

时间窗: 5 days

Reduction in inflammatory markers: CRP, ESR, NLR, PLR, plasma viscosity, lactate.

次要结局

  • Cancer recurrance(5 days)
  • Opioid use(5 days)
  • Anesthesia Dose(5 days)

研究者

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

Jason Wilson

Clinical Assistant Professor

University of British Columbia

研究点 (1)

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