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临床试验/NCT06683716
NCT06683716尚未招募不适用

Remote Assistance Via Smart Glasses Compared to In-person Assistance for Cannulation of the Native Papilla During Endoscopic Retrograde Cholangiopancreatography

Helios Kliniken Schwerin2 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2025年1月2日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
170
试验地点
2
主要终点
Papilla cannulation time

研究概览

简要总结

The aim of this prospective randomized study is to evaluate whether telemedical assistance via SmartGlasses is equivalent to physical presence in teaching Endoscopic Retrograde Cholangiopancreaticography (ERCP) in terms of examination success and safety. Endoscopic papilla cannulation is a key skill for successful ERCP and therefore a measurable primary endpoint of the study. This can be measured as the time (in seconds/minutes) between stable visualization of the papilla and successful endoscopic cannulation of the target structure (bile duct or pancreatic duct).

详细描述

In sparsely populated regions of a country and where there is a lack of experienced specialists, it may not always be possible to have an experienced ERCP examiner present during an examination. Therefore, telemedical examination assistance via a connection to data glasses worn by the examiner is a possible option to replace the physical presence of an instructor or experienced ERCP examiner.

The aim of this prospective randomized study is to evaluate whether telemedical assistance via smart glasses is equivalent to physical presence in terms of examination success and safety. Endoscopic papilla cannulation is a key skill for successful ERCP and therefore a measurable primary endpoint of the study. This can be measured as the time (in seconds/minutes) between stable visualization of the papilla and successful endoscopic cannulation of the target structure (bile duct or pancreatic duct).

In addition to other efficacy endpoints, adverse events, which are expected to be rare, will be documented at 48-hour intervals and calculated as a rate. Telemedical 'live' support of an ERCP via data glasses has not yet been demonstrated or tested in a trial. To ensure the safety of the examination under these circumstances, the training examiner is present in the neighbouring room and can physically assist or take over the examination at any time if necessary.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
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

入选标准

  • Adult patients aged ≥ 18 years without previous papillotomy

排除标准

  • Cannulation of the minor papilla necessary
  • Significant comorbidity
  • Haemodynamic instability
  • Pregnant women
  • Refusal or inability to give written informed consent for the study
  • Instructor had to perform the examination himself/herself

结局指标

主要结局

Papilla cannulation time

时间窗: During the intervention: from the stable visualisation of the papilla until the successful cannulation of the papilla, assessed up to 60 minutes

Time to cannulate the native papilla during ERCP

次要结局

  • Adverse events during and after ERCP(Time interval between insertion of the endoscope through the mouth up to 48 hours after ERCP)

研究者

发起方
Helios Kliniken Schwerin
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. med. Daniel Schmitz

Head physician of the Department of Gastroenterology

Helios Kliniken Schwerin

研究点 (2)

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