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COMPLETED NA

Vertos Mild - Post Market Patient Outcomes

NCT01076244 · View on ClinicalTrials.gov ↗

Study Summary

This is a single-center study evaluating the outcomes of patients with painful lumbar spinal stenosis who were treated with the mild procedure (minimally invasive lumbar decompression. The patients will be followed for 6 months after the procedure.

Conditions Studied

Interventions

  • PROCEDURE Minimally Invasive Lumbar Decompression

Study Locations (2)

West Virginia

  • The Center for Pain Relief, Inc. — Charleston
  • The Center for Pain Relief, Inc — Charleston

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2010-02
Est. Completion 2012-01
Phase NA

Sponsor

The Center for Pain Relief

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01076244

The ClinicalTrials.gov registry entry for NCT01076244 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 46 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Center for Pain Relief, which has 1 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 Lumbar Spinal Stenosis appearing as the primary indexed condition, and to 1 intervention — of which Minimally Invasive Lumbar Decompression 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: NCT01076244 reports 2 study locations spanning 1 distinct geographic area — top geographies include West Virginia. 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 NCT01076244 about?

NCT01076244 is a clinical study titled "Vertos Mild - Post Market Patient Outcomes". This is a single-center study evaluating the outcomes of patients with painful lumbar spinal stenosis who were treated with the mild procedure (minimally invasive lumbar decompression. The patients will be followed for 6 months after the procedure.

What is the current status of trial NCT01076244?

This trial is currently completed. It is a NA study. The enrollment target is 46 participants. The study started on 2010-02. Estimated completion is 2012-01.

What conditions does trial NCT01076244 study?

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

What interventions are being tested in trial NCT01076244?

The interventions under investigation include: Minimally Invasive Lumbar Decompression (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01076244?

This trial is sponsored by The Center for Pain Relief, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01076244 being conducted?

This trial has 2 study locations across West 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