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临床试验/NCT07246876
NCT07246876进行中(未招募)不适用

Diagnostic Value of EBUS-Guided Transbronchial Mediastinal Cryobiopsy Versus Conventional Bronchoscopic Approaches for Stage I/II Sarcoidosis

China-Japan Friendship Hospital1 个研究点 分布在 1 个国家目标入组 469 人开始时间: 2026年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
469
试验地点
1
主要终点
The granuloma detection rate

研究概览

简要总结

Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA), combined with endobronchial biopsy (EBB) and/or transbronchial lung biopsy (TBLB), and endobronchial ultrasound-guided transbronchial mediastinal cryobiopsy (EBUS-TBMC) have high diagnostic yields for patients with sarcoidosis. However, a direct comparison between them has not been conducted. This randomized controlled trial aims to compare directly the diagnostic yield between EBUS-TBMC and EBUS-TBNA+EBB+TBLB in sarcoidosis.

详细描述

Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA), combined with endobronchial biopsy (EBB) and/or transbronchial lung biopsy (TBLB), and endobronchial ultrasound-guided transbronchial mediastinal cryobiopsy (EBUS-TBMC) have high diagnostic yields for patients with sarcoidosis. However, a direct comparison between them has not been conducted. Two questions remain need to be answered: (1) Does EBUS-TBMC have the same or better diagnostic sensitivity for sarcoidosis than EBUS-TBNA combined with standard bronchoscopic modalities (EBB or/and TBLB)? (2) Can combining EBUS-TBMC with standard bronchoscopic modalities further increase the diagnostic sensitivity for sarcoidosis? This study is designed as a randomised controlled trial to compare the diagnostic yield between EBUS-TBMC and conventional bronchoscopic approaches for diagnosing stage I/II sarcoidosis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • •Age ≥18years;
  • •Patients with clinical and radiological suspicion of stage I or stage II sarcoidosis;
  • •Fully informed of the purpose and method of the study

排除标准

  • •Pathologically confirmed sarcoidosis, obvious organ involvement with the possibility of confirming granulomas using a minimally invasive diagnostic procedure;
  • •Patients with medical contraindications to bronchoscopy procedures.

研究组 & 干预措施

EBUS-TBNA

Experimental

Patients will receive endobronchial biopsy, transbronchial lung biopsy and EBUS-TBNA

干预措施: EBUS-TBNA-based sampling methods (Procedure)

EBUS-TBMC

Experimental

Patients will receive endobronchial biopsy, transbronchial lung biopsy and EBUS-TBMC

干预措施: EBUS-TBMC based sampling method (Procedure)

结局指标

主要结局

The granuloma detection rate

时间窗: 7 days after sampling

The number of patients with granulomas detected relative to the total number of patients tested.

次要结局

  • Negative predictive value(6 months after sampling)
  • Diagnostic yield(6 Month after sampling)
  • Incidence of complications(4 weeks after sampling)

研究者

发起方
China-Japan Friendship Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gang Hou

Principal Investigator

China-Japan Friendship Hospital

研究点 (1)

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