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ACTIVE NOT RECRUITING NA

Adaptix RCT Evaluating Adaptix™ Versus PEEK Cages

NCT05182489 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo combined interbody/posterolateral lumbar fusion procedures, supplemented with pedicle screw instrumentation, using one of the following interbody cages; the Medtronic Adaptix™ cage with roughened micro and nano-textured titanium surfaces or the CAPSTONE® poly-ether-ether-ketone cage.

Interventions

  • DEVICE Medtronic Adaptix™ titanium implants
  • DEVICE Medtronic CAPSTONE® PEEK cage

Study Locations (1)

Ohio

  • The Ohio State University Wexner Medical Center Neurological Surgery — Columbus

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2021-11-19
Est. Completion 2026-04-01
Phase NA

Sponsor

Ohio State University

640 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05182489

The ClinicalTrials.gov registry entry for NCT05182489 describes a study currently listed as active not recruiting. 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 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 640 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Degenerative Disc Disease appearing as the primary indexed condition, and to 2 interventions — of which Medtronic Adaptix™ titanium implants 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: NCT05182489 reports 1 study location spanning 1 distinct geographic area — top geographies include Ohio. 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 NCT05182489 about?

NCT05182489 is a clinical study titled "Adaptix RCT Evaluating Adaptix™ Versus PEEK Cages". The purpose of this randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo combined interbody/posterolateral lumbar fusion procedures, supplemented with pedicle screw instrumentation, using one of the following interbody cages; the Medt...

What is the current status of trial NCT05182489?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2021-11-19. Estimated completion is 2026-04-01.

What conditions does trial NCT05182489 study?

This clinical trial studies the following conditions: Degenerative Disc Disease, Spondylolisthesis, Spinal Canal Stenosis, Osteophyte, Bony Growth Formation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05182489?

The interventions under investigation include: Medtronic Adaptix™ titanium implants (DEVICE), Medtronic CAPSTONE® PEEK cage (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05182489?

This trial is sponsored by Ohio State University, which has 640 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05182489 being conducted?

This trial has 1 study location across Ohio. 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