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NCT01936467 · ClinicalTrials.gov registry record · Phase 3
Comparison of Two Needle Aspiration Techniques for Endoscopic Ultrasound-guided Fine Needle Aspiration (EUS-FNA) in Solid Pancreatic Lesions
A Phase 3 study of Pancreatic Solid Lesions and Pancreatic Mass, sponsored by Johns Hopkins University.
- Completed
- Registry status
- Phase 3
- Development phase
- 121
- Enrollment target
- 2
- Study locations
NCT01936467 is a Phase 3 study of Pancreatic Solid Lesions and Pancreatic Mass that has completed, run by Johns Hopkins University. The registered enrollment target is 121 participants. The trial reports 2 study locations across 1 state.
The verdict
NCT01936467, a Phase 3 study of Pancreatic Solid Lesions and Pancreatic Mass, has completed, sponsored by Johns Hopkins University.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 121 participants
- Enrollment target
- 2
- Study locations
Study Summary
The aim of this study is to compare Endoscopic Ultrasound and Fine Needle Aspirate with a standard 22-gauge needle using either "standard-suction" or "capillary suction" methods for solid pancreatic lesions. Investigators hope to discover the best technique for obtaining diagnostic material when patients with a pancreatic mass undergo endoscopic ultrasound and fine needle aspirate procedure. There are currently several techniques for obtaining tissue during endoscopic ultrasound and fine needle aspirate. The procedure will be performed by either the capillary suction technique or no suction technique.
Conditions Studied
Interventions
- DEVICE Standard technique EUS-FNA
- DEVICE Capillary suction technique for EUS FNA
Study Locations (2)
Maryland
- Johns Hopkins Hospital - Baltimore
- Howard County General Hospital - Columbia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 121 participants |
| Start Date | 2013-01 |
| Est. Completion | 2015-01 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01936467
The ClinicalTrials.gov registry entry for NCT01936467 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 121 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pancreatic Solid Lesions appearing as the primary indexed condition, and to 2 interventions - of which Standard technique EUS-FNA is the first listed.
NCT01936467 reports 2 study locations spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT01936467 about?
NCT01936467 is a clinical study titled "Comparison of Two Needle Aspiration Techniques for Endoscopic Ultrasound-guided Fine Needle Aspiration (EUS-FNA) in Solid Pancreatic Lesions". The aim of this study is to compare Endoscopic Ultrasound and Fine Needle Aspirate with a standard 22-gauge needle using either "standard-suction" or "capillary suction" methods for solid pancreatic lesions. Investigators hope to discover the best technique for obtaining diagnostic material when pat...
What is the current status of trial NCT01936467?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 121 participants. The study started on 2013-01. Estimated completion is 2015-01.
What conditions does trial NCT01936467 study?
This clinical trial studies the following conditions: Pancreatic Solid Lesions, Pancreatic Mass.
What interventions are being tested in trial NCT01936467?
The interventions under investigation include: Standard technique EUS-FNA (DEVICE), Capillary suction technique for EUS FNA (DEVICE).
Who is sponsoring clinical trial NCT01936467?
This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01936467 being conducted?
This trial has 2 study locations across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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