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A prospective randomized comparative study of the difference in cytopathologic diagnosis between EUS-FNA with or without suction in pancreatic and peripancreatic masses

Not Applicable
Recruiting
Conditions
Neoplasms
Registration Number
KCT0000878
Lead Sponsor
Asan Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
56
Inclusion Criteria

Patients with pancreatic or peri-pancreatic solid masses who need EUS-FNA for diagnosis

Exclusion Criteria

1) Age < 19
2) Ongoing gastrointestinal bleeding
3) Coagulation disorder (platelet < 50,000/mm3 and/or prothrombin time international normalized ratio(PT INR) > 1.5)
4) In use of Thienopyridine (e.g. clopidogrel)
5) Refusal to provide informed consent

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Diagnostic accuracy
Secondary Outcome Measures
NameTimeMethod
Sample quality (cellularity, number of cells per slide, adequacy of specimen, blood contamination)
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