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Short Term Pancreatic Stenting Registry

NCT02262845 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to document clinical utility and distribution of indications for short term pancreatic stenting, and stent type preference by indication at tertiary referral centers with expertise in pancreatic endotherapy.

Interventions

  • DEVICE The Advanix™ Pancreatic Stent and NaviFlex RX Pancreatic Delivery System and Pushers

Study Locations (7)

Other

  • Evangelisches Krankenhaus Dusseldorf — Düsseldorf
  • Erasmus Medical Center — Rotterdam

Pennsylvania

  • Temple University School of Medicine — Philadelphia

South Carolina

  • Medical University of South Carolina — Charleston

Texas

  • Methodist Dallas Medical Center — Dallas

Washington

  • Virginia Mason Medical Center — Seattle

Hyderabad

  • Asian Institute of Gastroenterology — Somājigūda

Trial Details

FieldValue
Enrollment Target 246 participants
Start Date 2015-02
Est. Completion 2016-09

Sponsor

Boston Scientific Corporation

120 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02262845

The ClinicalTrials.gov registry entry for NCT02262845 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 246 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Scientific Corporation, which has 120 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Post-ERCP Acute Pancreatitis appearing as the primary indexed condition, and to 1 intervention — of which The Advanix™ Pancreatic Stent and NaviFlex RX Pancreatic Delivery System and Pushers is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02262845 reports 7 study locations spanning 6 distinct geographic areas — top geographies include Other, Pennsylvania, South Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02262845 about?

NCT02262845 is a clinical study titled "Short Term Pancreatic Stenting Registry". The purpose of this study is to document clinical utility and distribution of indications for short term pancreatic stenting, and stent type preference by indication at tertiary referral centers with expertise in pancreatic endotherapy.

What is the current status of trial NCT02262845?

This trial is currently completed. The enrollment target is 246 participants. The study started on 2015-02. Estimated completion is 2016-09.

What conditions does trial NCT02262845 study?

This clinical trial studies the following conditions: Post-ERCP Acute Pancreatitis, Pancreatic Duct Stricture, Pancreatic Duct Stones, Pancreatic Duct Leakage. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02262845?

The interventions under investigation include: The Advanix™ Pancreatic Stent and NaviFlex RX Pancreatic Delivery System and Pushers (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02262845?

This trial is sponsored by Boston Scientific Corporation, which has 120 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02262845 being conducted?

This trial has 7 study locations across Pennsylvania, South Carolina, Texas, Washington, Hyderabad. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial