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COMPLETED Phase 4

Randomized Study of Anular Repair With the Xclose Tissue Repair System

NCT00760799 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the benefits of anulus fibrosus repair utilizing Xclose™ compared to a discectomy without anulus fibrosus repair.

Conditions Studied

Interventions

  • PROCEDURE Discectomy with anular repair

Study Locations (20)

Florida

  • North Florida Regional Hospital — Gainesville
  • Lyerly Neurosurgical (Baptist Health) — Jacksonville
  • Mayo Clinic — Jacksonville
  • Lyerly Neurosurgical (Centerone) — Jacksonville

Illinois

  • Midwest Orthopaedics at Rush — Chicago
  • Chicago Institute of Neurosurgery and Neuroresearch — Chicago
  • Palos Community Hospital — Palos Heights

Arizona

  • Texas Back Institute — Phoenix
  • Desert Institute for Spine Care — Phoenix

Colorado

  • Denver Spine (Porter Hospital) — Greenwood Village
  • Denver Spine (Presbyterian/St. Luke's Hospital) — Greenwood Village

Michigan

  • Oakwood Hospital — Dearborn
  • Henry Ford — Detroit

Alabama

  • North Alabama Neurological, P.A. — Huntsville

California

  • University of California San Diego — San Diego

Indiana

  • Indiana Spine Group — Indianapolis

Trial Details

FieldValue
Enrollment Target 750 participants
Start Date 2007-03
Est. Completion 2012-01
Phase Phase 4

Sponsor

Anulex Technologies

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00760799

The ClinicalTrials.gov registry entry for NCT00760799 describes a study currently listed as completed. It is categorized as Phase 4, 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 750 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Anulex Technologies, 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 Diskectomy appearing as the primary indexed condition, and to 1 intervention — of which Discectomy with anular repair 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: NCT00760799 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Florida, Illinois, Arizona. 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 NCT00760799 about?

NCT00760799 is a clinical study titled "Randomized Study of Anular Repair With the Xclose Tissue Repair System". The purpose of this study is to evaluate the benefits of anulus fibrosus repair utilizing Xclose™ compared to a discectomy without anulus fibrosus repair.

What is the current status of trial NCT00760799?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 750 participants. The study started on 2007-03. Estimated completion is 2012-01.

What conditions does trial NCT00760799 study?

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

What interventions are being tested in trial NCT00760799?

The interventions under investigation include: Discectomy with anular repair (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00760799?

This trial is sponsored by Anulex Technologies, 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 NCT00760799 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. 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