Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01815606 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by AdventHealth.

Completed
Registry status
NA
Development phase
51
Enrollment target

NCT01815606: Completed NA study, sponsored by AdventHealth.

NCT01815606 is a NA study that has completed, run by AdventHealth. The registered enrollment target is 51 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01815606, a NA study, has completed, sponsored by AdventHealth.

COMPLETED
Registry status
NA
Development phase
51 participants
Enrollment target

Study Summary

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.

Primary Outcome

The use of a 19G FNA needle reduces the number of passes required to establish a diagnosis in pancreatic tumors that are greater than 35mm in size. This translates to less sedation, faster patient recovery, better safety and time efficiency.

Interventions

  • PROCEDURE biopsy with 19 gauge needle
  • PROCEDURE biopsy with 25 gauge needle

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2013-02
Est. Completion 2013-12
Phase NA
AdventHealth

95 total trials

What the finished NCT01815606 record still lists

NCT01815606 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which biopsy with 19 gauge needle is the first listed.

NCT01815606 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01815606 about?

NCT01815606 is a clinical study titled "Trial Comparing 19 and 25G Needles for Fine Needle Aspiration (FNA) of Solid Pancreatic Mass Lesions Greater Than 35mm". 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 bio...

What is the current status of trial NCT01815606?

This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2013-02. Estimated completion is 2013-12.

What interventions are being tested in trial NCT01815606?

The interventions under investigation include: biopsy with 19 gauge needle (PROCEDURE), biopsy with 25 gauge needle (PROCEDURE).

Who is sponsoring clinical trial NCT01815606?

This trial is sponsored by AdventHealth, which has 95 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01815606's enrollment target sits among peer trials

51 1279th of 2000 higher than 722 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02701153 · 51 participants · NA

    Phase II Study of 5-Day Hypofractionated Preoperative Radiation Therapy for Soft Tissue Sarcomas: Expansion Cohort

  • NCT03663790 · 51 participants · NA

    Effects of Gait Retraining on Lower Extremity Biomechanics

  • NCT03874052 · 51 participants · Phase 1

    Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

  • NCT04704661 · 51 participants · Phase 1

    Testing the Combination of Two Anti-cancer Drugs, DS-8201a and AZD6738, for The Treatment of Advanced Solid Tumors Expressing the HER2 Protein or Gene, The DASH Trial

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01815606, the US trial registry maintained by the National Library of Medicine. NCT01815606 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.