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NCT00760799 · ClinicalTrials.gov registry record · Phase 4

Randomized Study of Anular Repair With the Xclose Tissue Repair System

A Phase 4 study of Diskectomy, sponsored by Anulex Technologies.

Completed
Registry status
Phase 4
Development phase
750
Enrollment target
20
Study locations

NCT00760799: Completed Phase 4 study of Diskectomy, sponsored by Anulex Technologies.

NCT00760799 is a Phase 4 study of Diskectomy that has completed, run by Anulex Technologies. The registered enrollment target is 750 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (45% higher). The trial reports 20 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00760799, a Phase 4 study of Diskectomy, has completed, sponsored by Anulex Technologies.

COMPLETED
Registry status
Phase 4
Development phase
750 participants
Enrollment target
20
Study locations

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
Anulex Technologies

1 total trials

What the finished NCT00760799 record still lists

NCT00760799 is an interventional study that assigns participants to a tested intervention. The registered 750 participants enrollment target is mid-sized for trials with a published cap, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (45% higher).

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.

NCT00760799 names 20 study sites across 12 states, led by Florida, Illinois, Arizona.

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.

What interventions are being tested in trial NCT00760799?

The interventions under investigation include: Discectomy with anular repair (PROCEDURE).

Who is sponsoring clinical trial NCT00760799?

This trial is sponsored by Anulex Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov.

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.

Similar trials for Diskectomy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00760799's enrollment target sits among peer trials

750 108th of 2000 higher than 1,891 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00760799, the US trial registry maintained by the National Library of Medicine. NCT00760799 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.