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Trial Comparing 19 and 25G Needles for Fine Needle Aspiration (FNA) of Solid Pancreatic Mass Lesions Greater Than 35mm

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AdventHealth

Status

Completed

Conditions

Pancreatic Cancer

Treatments

Procedure: biopsy with 25 gauge needle
Procedure: biopsy with 19 gauge needle

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study will test two different needles for performing a biopsy of the pancreas during endoscopic ultrasound (EUS) procedures. Patients who are asked to participate in this study have a growth in the pancreas measuring greater than 35mm that needs a biopsy so that a diagnosis can be made. The biopsy can be performed using either a 19 or 25-Gauge needle. The purpose of this study is to compare which of the two needles is better for performing biopsies of the pancreas on masses that are greater than 35mm.

Full description

Endoscopic Ultrasound-guided fine needle aspiration (EUS-FNA) can be performed using the 25, 22 or 19 gauge (G) needles. Randomized trials have shown that all three needles are safe and perform equally well. However, in a retrospective study, the diagnostic sensitivity of EUS-FNA for pancreatic masses that measured more than 35mm was less compared to smaller size masses. This is because larger size tumors have more necrosis and it is difficult to identify cancer cells in them to make a diagnosis. Therefore, more biopsies must be performed in larger size tumors to establish a diagnosis. In previous studies it has been shown that the larger 19G needles procure larger and better quality tissue. Therefore, our hypothesis is that, when a larger 19G needle is used to FNA tumors more than 35mm, a diagnosis can be achieved with fewer passes.

Enrollment

51 patients

Sex

All

Ages

19 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

All patients referred to Florida Hospital Endoscopy Unit for assessment of pancreatic mass lesions greater than 35 mm on computed tomography (CT) that require FNA.

Exclusion criteria

  • Age < 19 years
  • Unable to safely undergo EUS for any reason
  • Coagulopathy (INR >1.6, Prothrombin Time >18secs, Thrombocytopenia <80,000 cells/ml)
  • Unable to consent
  • Non-English speaking patients
  • Participation in any other clinical trial (excluding registries or databases)

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

51 participants in 2 patient groups

19 Gauge needle biopsy
Active Comparator group
Description:
biopsy with 19 gauge needle
Treatment:
Procedure: biopsy with 19 gauge needle
25 gauge needle biopsy
Active Comparator group
Description:
biopsy with 25 gauge needle
Treatment:
Procedure: biopsy with 25 gauge needle

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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