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RECRUITING Phase 1

Initial Feasibility Study to Treat Borderline Resectable Pancreatic Cancer With a Planar LDR Source

NCT02843945 · View on ClinicalTrials.gov ↗

Study Summary

Initial study to evaluate local control and the preferred method of attachment of the CivaSheet in the setting of suspected close or positive margins at the time of surgical tumor removal.

Conditions Studied

Interventions

  • DEVICE Directional Brachytherapy Source Implant

Study Locations (6)

Illinois

  • Rush University Cancer Center — Chicago
  • Advocate Christ Medical Center — Oak Lawn

Florida

  • Tampa General Hospital — Tampa

Louisiana

  • University Medical Center LSU — New Orleans

Pennsylvania

  • Fox Chase Cancer Center — Philadelphia

Virginia

  • Virginia Commonwealth University Massey Cancer Center — Richmond

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2017-05-31
Est. Completion 2028-10-30
Phase Phase 1

Sponsor

CivaTech Oncology

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02843945

The ClinicalTrials.gov registry entry for NCT02843945 describes a study currently listed as recruiting. It is categorized as Phase 1, 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 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CivaTech Oncology, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Pancreatic Cancer appearing as the primary indexed condition, and to 1 intervention — of which Directional Brachytherapy Source Implant 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: NCT02843945 reports 6 study locations spanning 5 distinct geographic areas — top geographies include Illinois, Florida, Louisiana. 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 NCT02843945 about?

NCT02843945 is a clinical study titled "Initial Feasibility Study to Treat Borderline Resectable Pancreatic Cancer With a Planar LDR Source". Initial study to evaluate local control and the preferred method of attachment of the CivaSheet in the setting of suspected close or positive margins at the time of surgical tumor removal.

What is the current status of trial NCT02843945?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2017-05-31. Estimated completion is 2028-10-30.

What conditions does trial NCT02843945 study?

This clinical trial studies the following conditions: Pancreatic Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02843945?

The interventions under investigation include: Directional Brachytherapy Source Implant (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02843945?

This trial is sponsored by CivaTech Oncology, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02843945 being conducted?

This trial has 6 study locations across Florida, Illinois, Louisiana, Pennsylvania, Virginia. 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