Clin2
NCT07677982Possibly a fitRecruiting

Understanding consent and sedation needs for endobronchial ultrasound

ENDOBRONCHIAL ULTRASOUND - TRANSBRONCHIAL NEEDLE ASPIRATIONProcedural Sedation and AnalgesiaInformed Consent

Part of Brain & nervous system clinical trials.

This study looks at how well patients understand the consent process and how much sedative medication they need during an endobronchial ultrasound (a scope test to look at the lungs and lymph nodes). It aims to improve care for people undergoing this procedure.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
75 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years or older
  • You are scheduled for an endobronchial ultrasound (a lung scope test)
  • You are generally healthy or have mild to moderate health problems (ASA class I to III)
  • You can read and understand Turkish
  • You agree to take part in the study
  • You do not have an active psychiatric illness that affects communication or understanding
  • You do not have dementia, delirium, or other cognitive issues
  • You are not allergic to propofol, midazolam, or remifentanil
  • You have not used anxiety or sedation medicines regularly in the last month
  • You do not have severe organ failure or unstable health that could affect sedation or communication

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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