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临床试验/NCT02704078
NCT02704078已完成不适用

Prospective Randomized Comparison of Trans-tracheal (EBUS-TBNA) Versus Trans-esophageal (EUS-B-FNA) Route as the Primary Approach for Fine Needle Aspiration of Mediastinal Lesions Using the Convex Probe Endobronchial Ultrasound (EBUS) Scope

All India Institute of Medical Sciences, New Delhi2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2015年12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
已完成
发起方
入组人数
100
试验地点
2
主要终点
Diagnostic Sensitivity of EUS-B-FNA versus EBUS-TBNA

研究概览

简要总结

Endobronchial Ultrasound Guided Transbronchial Needle aspiration (EBUS-TBNA) is a firmly established modality for diagnostic evaluation of mediastinal lesions. The procedure is routinely performed at the Department of Pulmonary Medicine and Sleep Disorders, AIIMS, New Delhi since 2012. Transesophageal approach for fine needle aspiration of mediastinal lesions using the Endobronchial Ultrasound (EBUS) scope [also described as Transesophageal Bronchoscopic Ultrasound Guided Fine Needle aspiration (EUS-B-FNA)] (also routinely performed in the department) and has been described as a safe and efficacious modality. EUS-B-FNA is usually employed when EBUS-TBNA is not feasible or excessive cough or secretions necessitate switch to esophageal route. We hypothesize that EUS-B-FNA as the primary approach has similar diagnostic performance as EBUS-TBNA and is associated with greater patient and operator rated procedure comfort and lesser requirement of anaesthesia medications for evaluation of patients with mediastinal lesions easily accessible with either of the two approaches.

We propose to undertake a prospective randomized comparison of Transesophageal (EUS-B-FNA) versus Transtracheal (EBUS-TBNA) approach for fine needle aspiration using the same EBUS scope in patients referred for endo-sonographic evaluation of mediastinal lesions. A total of 100 serial patients (with Subcarinal and/or Lower Left paratracheal located mediastinal lymphadenopathy at least >1cm in Short axis diameter) shall be included. After consent and preliminary investigations, patients shall be randomized equally into the two approaches. Procedure will be performed under local anaesthesia (topical lignocaine) and i.v. sedation (midazolam and fentanyl) in the bronchoscopy laboratory. The primary objective will be comparison of proportion of diagnostic and adequate aspirates in the two groups. Secondary objectives will include operator rated cough (VAS), Operator rated overall procedure satisfaction (VAS), dose of midazolam and fentanyl administered, lignocaine dose and total procedure duration.The primary data analysis shall be for the performance characteristics of the primary approach. All the aspirates shall be analysed by the same pathologist for final interpretation.

详细描述

Objectives

Primary objective:

Comparison of Proportion of Adequate and Diagnostic Aspirates in the EUS-B-FNA versus EBUS-TBNA arms as the primary approach for mediastinal fine needle aspiration during Convex probe EBUS.

Secondary objectives

  1. Topical Anaesthetic requirement between the two groups
  2. Intravenous Sedative / analgesic requirement between the two groups
  3. Operator rated overall procedure satisfaction (VAS)
  4. Operator rated cough (VAS)
  5. Overall duration of procedure Methods Study Design: Prospective randomised study. Sample Size: Number of Patients: 100 (50 -EBUS-TBNA arm, 50- EUS-B-FNA arm)

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
Single (Participant)

入排标准

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

入选标准

  • Age 18 years and Older
  • Predominant Subcarinal or Lower Left paratracheal located mediastinal lymphadenopathy/mediastinal lesions at least >1cm in Short axis diameter.
  • Patients who give consent

排除标准

  • Refusal of consent for the procedure
  • Any contraindications to Bronchoscopy / Endobronchial Ultrasound
  • Pregnancy

研究组 & 干预措施

EBUS-TBNA

Active Comparator

Mediastinal lymph node aspiration shall be performed transtracheally.

干预措施: EBUS-TBNA (Device)

EUS-B-FNA

Experimental

Mediastinal lymph node aspiration shall be performed transesophageally

干预措施: EUS-B-FNA (Device)

结局指标

主要结局

Diagnostic Sensitivity of EUS-B-FNA versus EBUS-TBNA

时间窗: At study completion at approximately 18 months

The diagnostic yield of EBUS-TBNA shall be compared with EUS-B-FNA ie comparison of the proportion of diagnostic aspirates between the EBUS-TBNA and the EUS-B-FNA groups

次要结局

  • Topical Anaesthetic requirement between the two groups(Comparing the mean doses of lignocaime administered in mg between the study participants in two groups at study completion at approximately 18 months)
  • Intravenous Sedative / analgesic requirement between the two groups(Compating the mean doses of sedative administered in mg between the study participants in two groups at study completion at approximately 18 months)
  • Operator rated overall procedure satisfaction (VAS)(At study completion at approximately 18 months)
  • Operator rated cough between the two procedures (VAS)(At study completion at approximately 18 months)
  • Overall duration of procedure(Intraoperative)

研究者

发起方
All India Institute of Medical Sciences, New Delhi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Karan Madan

Dr. Karan Madan, MD, DM Assistant Professor, Pulmonary MedicIne and Sleep Disorders

All India Institute of Medical Sciences, New Delhi

研究点 (2)

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