Your session is about to expire
← Back to Search
Procedure
Needle Comparison for Diagnosing Sarcoidosis
N/A
Recruiting
Led By Kazuhiro Yasufuku
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Patients that are unable to provide informed consent
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 years
Awards & highlights
No Placebo-Only Group
Summary
This trial wants to see if using Franseen-type needles for sample collection can help diagnose sarcoidosis better than the conventional Menghini-type needle.
Who is the study for?
This trial is for individuals with sarcoidosis, a condition where tiny clumps of inflammatory cells grow in different parts of the body. Participants should be suitable candidates for a procedure called EBUS-TBNA, which collects tissue samples from the lungs.
What is being tested?
The study is testing two types of needles used in EBUS-TBNA: Franseen-type and Menghini-type. It aims to determine if the Franseen needle provides better quality samples for diagnosing sarcoidosis compared to the conventional Menghini needle.
What are the potential side effects?
EBUS-TBNA may cause coughing, bleeding at puncture sites, infection risk, shortness of breath or discomfort during and after the procedure. The side effects can vary based on individual patient factors.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am unable to understand or sign the consent form.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Rate of adequate tissue sampling from lymph nodes (as determined by pathologists)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Menghini-type needleExperimental Treatment1 Intervention
the standard needle type
Group II: Franseen-type needlesActive Control1 Intervention
the active comparator arm
Find a Location
Who is running the clinical trial?
University Health Network, TorontoLead Sponsor
1,521 Previous Clinical Trials
503,176 Total Patients Enrolled
1 Trials studying Sarcoidosis
40 Patients Enrolled for Sarcoidosis
Kazuhiro YasufukuPrincipal InvestigatorUHN
Share this study with friends
Copy Link
Messenger