Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06368245 · ClinicalTrials.gov registry record

Durability of Suppl. Rod Constructs-SuppleMentAry Rod Technique for Long-segment Posterior Instrumented Spinal Fusions

A clinical trial of Spinal Fusion, sponsored by AO Foundation, AO Spine.

Recruiting
Registry status
1,244
Enrollment target
17
Study locations

NCT06368245: Recruiting study of Spinal Fusion, sponsored by AO Foundation, AO Spine.

NCT06368245 is a study of Spinal Fusion that is actively recruiting participants, run by AO Foundation, AO Spine. The registered enrollment target is 1,244 participants, above the 418-participant average among 19 other Spinal Fusion trials with a reported enrollment target (198% higher). The trial reports 17 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06368245, a study of Spinal Fusion, is actively recruiting participants, sponsored by AO Foundation, AO Spine.

RECRUITING
Registry status
1,244 participants
Enrollment target
17
Study locations

Study Summary

This is a multicenter retrospective comparative cohort study. The index surgery for this study is primary or revision long-segment posterior thoracolumbar (TL) instrumented fusion using either a supplementary rod construct or a dual-rod construct. Eligible patients who already had index surgery, will be identified for enrollment through a review of medical records of the participating surgeons at the study sites.

Primary Outcome

Incidence of rod fracture(s)

Conditions Studied

Interventions

  • PROCEDURE long-segment posterior TL instrumented fusion

Study Locations (17)

Other

  • University of Calgary Spine - Calgary
  • University of Toronto - Toronto
  • Duchess of Kent Children's Hospital - Hong Kong
  • Kothari Medical Centre - Kolkata
  • Hamamatsu University School of Medicine - Hamamatsu
  • University of Tokyo - Tokyo
  • Hospital Vall d´Hebron - Barcelona
  • Acibadem Maslak Hospital - Istanbul

California

  • Stanford Spine Clinic - Redwood City
  • University of California - Sacramento
  • UCSF Spine Center - San Francisco

Missouri

  • Washington University in St. Louis, School of Medicine - St Louis
  • Washington University in St. Louis, School of Medicine, Saint Louis, Missouri 63110 - St Louis

Maryland

  • John Hopkis Hospital - Baltimore

Minnesota

  • University of Minnesota Medical Center - Minneapolis

New York

  • Columbia University / NYP Och Spine Hospital - New York

Virginia

  • University of Virginia - Charlottesville

Trial Details

FieldValue
Enrollment Target 1,244 participants
Start Date 2025-03-24
Est. Completion 2029-07-31
AO Foundation, AO Spine

9 total trials

What NCT06368245 shows while recruiting

NCT06368245 is an observational study that tracks outcomes without assigning an intervention. Its 1,244 participants enrollment target places it among the larger protocols in the corpus, above the 418-participant average among 19 other Spinal Fusion trials with a reported enrollment target (198% higher).

The record links to 1 condition, with Spinal Fusion appearing as the primary indexed condition, and to 1 intervention - of which long-segment posterior TL instrumented fusion is the first listed.

NCT06368245 lists 17 locations in 7 states (Other, California, Missouri).

Frequently Asked Questions

What is clinical trial NCT06368245 about?

NCT06368245 is a clinical study titled "Durability of Suppl. Rod Constructs-SuppleMentAry Rod Technique for Long-segment Posterior Instrumented Spinal Fusions". This is a multicenter retrospective comparative cohort study. The index surgery for this study is primary or revision long-segment posterior thoracolumbar (TL) instrumented fusion using either a supplementary rod construct or a dual-rod construct. Eligible patients who already had index surgery, wil...

What is the current status of trial NCT06368245?

This trial is currently recruiting. The enrollment target is 1,244 participants. The study started on 2025-03-24. Estimated completion is 2029-07-31.

What conditions does trial NCT06368245 study?

This clinical trial studies the following conditions: Spinal Fusion.

What interventions are being tested in trial NCT06368245?

The interventions under investigation include: long-segment posterior TL instrumented fusion (PROCEDURE).

Who is sponsoring clinical trial NCT06368245?

This trial is sponsored by AO Foundation, AO Spine, which has 9 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06368245 being conducted?

This trial has 17 study locations across California, Maryland, Minnesota, Missouri, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Spinal Fusion

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 NCT06368245's enrollment target sits among peer trials

1,244 2nd of 19 the highest of 19 other Spinal Fusion trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Spinal Fusion 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02743858 · 1,250 participants

    Lymphedema Surveillance Study

  • NCT04670874 · 1,250 participants

    Quality of Life in Cutaneous Lymphoma Patients Using the Skindex29

  • NCT04807868 · 1,250 participants

    AdventHealth Research Institute Non-Alcoholic Fatty Liver Disease Biobank and Registry (AVAIL)

  • NCT05995821 · 1,250 participants

    Immunobiology Blood and Tissue Collection of Upper Aerodigestive Malignancies

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06368245, the US trial registry maintained by the National Library of Medicine. NCT06368245 (large enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.