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Clinical Trials/KCT0000722
KCT0000722
Recruiting
未知

sefulness of EUS-guided 22-gauge ProCore needle biopsy with capillary sampling for intra-abdominal mass

Asan Medical Center0 sites150 target enrollmentTBD
ConditionsNeoplasms

Overview

Phase
未知
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Asan Medical Center
Enrollment
150
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Observational Study
Sex
All

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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