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Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therapy During the Trial
NCT03277378 · View on ClinicalTrials.gov ↗
Study Summary
Prospective, multi-center, randomized, single blind study
Conditions Studied
Interventions
- DEVICE lead placement followed by BurstDR stimulation
Study Locations (20)
Other
- Frankston Pain Management — Frankston
- North Shore Private Hospital — Saint Leonards
- Hospital Elisabethinen GmbH — Graz
- Wilhelminenspital Wien — Vienna
- Sana Kliniken Duisburg Gm.bH — Duisburg
- Medizinische Einrichtungen der Universität Düsseldorf — Düsseldorf
- Hospital Gera -Zentrum für interdisziplinäre Schmerztherapie — Gera
Florida
- Comprehensive Spine Institute — Clearwater
- Florida Pain Institute — Merritt Island
- National Pain Institute Winter Park — Winter Park
Nevada
- Advanced Pain Care — Las Vegas
- Nevada Advanced Pain Specialists — Reno
Oregon
- Oregon Health & Science University — Portland
- Spinal Diagnostics — Tualatin
California
- Jason Edward Pope, MD — Santa Rosa
Illinois
- Rush University — Chicago
Kansas
- Kansas University Medical Center — Kansas City
Rhode Island
- Rhode Island Hospital — Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 270 participants |
| Start Date | 2017-09-22 |
| Est. Completion | 2018-10-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03277378
The ClinicalTrials.gov registry entry for NCT03277378 describes a study currently listed as completed. It is categorized as NA, 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 270 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 155 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 Chronic, Intractable Pain of the Trunk and/or Lower Limbs appearing as the primary indexed condition, and to 1 intervention — of which lead placement followed by BurstDR stimulation 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: NCT03277378 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Other, Florida, Nevada. 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 NCT03277378 about?
NCT03277378 is a clinical study titled "Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therapy During the Trial". Prospective, multi-center, randomized, single blind study
What is the current status of trial NCT03277378?
This trial is currently completed. It is a NA study. The enrollment target is 270 participants. The study started on 2017-09-22. Estimated completion is 2018-10-12.
What conditions does trial NCT03277378 study?
This clinical trial studies the following conditions: Chronic, Intractable Pain of the Trunk and/or Lower Limbs. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03277378?
The interventions under investigation include: lead placement followed by BurstDR stimulation (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03277378?
This trial is sponsored by Abbott Medical Devices, which has 155 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03277378 being conducted?
This trial has 20 study locations across California, Florida, Illinois, Kansas, Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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