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临床试验/NCT06610071
NCT06610071尚未招募1 期

Near-infrared Fluorescence Image-guided Surgery for Malignant Soft Tissue Tumor With Low-dose Second Window Indocyanine Green Technique: a Multicenter Randomized Controlled Trial

The Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College0 个研究点目标入组 592 人开始时间: 2024年10月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
592
主要终点
2-year local recurrence rate

研究概览

简要总结

This research study will evaluate how near-infrared fluorescence (NIRF) imaging with low-dose second window indocyanine green (ICG) can assist in the radical resection and pathologic diagnosis of malignant soft tissue sarcoma, such as dermatofibrosarcoma protuberans (DFSP) and skin squamous cell carcinoma (sSCC) during surgery.

详细描述

To improve the accuracy of radical resection by reducing the risk of missed diagnosis of positive margin, this study will explore clinical application of near-infrared fluorescence imaging with modified low-dose SWIG technique in guiding radical resection of malignant soft tissue tumor. The investigators conduct a multi-center, multi-subgroup, prospective randomized controlled trial. The participants will be first stratified according to histological type involving dermatofibrosarcoma protuberans (DFSP) and skin squamous cell carcinoma (sSCC). The patients with DFSP or sSCC will be then randomly assigned to three groups. Patients in the control group will not receive ICG administration. The ICG was injected intravenously 24 hours before surgery, at a dose of 0.25 mg/kg in the first experimental group and 25 mg/patient in the second experimental group, respectively. The patients in the control groups will undergo traditional assessment of surgical margins.The patients in the experimental groups, on the other hand, will be scheduled to intraoperative near-infrared fluorescence imaging to scan gross tumor, tumor bed and cross-sectional specimen. The 2-year local recurrence rate will be regarded as primary outcome. The number of positive margins will be compared among groups. The investigators will also calculate the sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) with 95% confidence intervals based on fluorescent signal of tumor bed in the experimental groups.

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, Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with DFSPs or sSCC in heads, extremities or trunk

排除标准

  • seafood/iodine allergy
  • hyperthyroidism
  • pregnancy
  • myasthenia gravis
  • acute severe hypertension

研究组 & 干预措施

Patients with DFSP in the first experimental group

Experimental

The ICG was injected intravenously 24 hours before surgery at a dose of 0.25 mg/kg in the first experimental group.

干预措施: ICG administration (Drug)

Patients with DFSP in the second experimental group

Experimental

The ICG was injected intravenously 24 hours before surgery at a dose of 25 mg/patient in the second experimental group.

干预措施: ICG administration (Drug)

Patients with sSCC in the first experimental group

Experimental

The ICG was injected intravenously 24 hours before surgery at a dose of 0.25 mg/kg in the first experimental group.

干预措施: ICG administration (Drug)

Patients with sSCC in the second experimental group

Experimental

The ICG was injected intravenously 24 hours before surgery at a dose of 25 mg/patient in the second experimental group.

干预措施: ICG administration (Drug)

结局指标

主要结局

2-year local recurrence rate

时间窗: up to 24 months

次要结局

  • number of positive margins(through study completion, an average of 2 years)
  • sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV)(through study completion, an average of 2 years)
  • Adverse effects(through study completion, an average of 2 years)

研究者

发起方
The Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
申办方类型
Other
责任方
Principal Investigator
主要研究者

Lei Cui

Principal Investigator

The Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

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