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sefulness of 22G ProCore fine needle biopsy with capillary sampling

Not Applicable
Recruiting
Conditions
Neoplasms
Registration Number
KCT0000722
Lead Sponsor
Asan Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
150
Inclusion Criteria

Patients with intra-abdominal mass who needed EUS-guided fine needle biopsy to confirm the pathological diagnosis

Exclusion Criteria

#1 Patients with bleeding tendency
#2 Hemodynamically unstable patients
#3 patients whose life expectancy is less than 1 month
#4 When informed consent was not obtained

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Diagnostic sensitivity, specificity, positive predictive value, negative predictive value and accuracy
Secondary Outcome Measures
NameTimeMethod
Procedure-related adverse event
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