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

RECRUITING

OssDsign® Spine Registry Study ("Propel")

NCT05329129 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this multi-center, prospective, observational registry is to gather information on the clinical outcomes and real-world use of commercially available bone graft substitutes manufactured by OssDsign® AB, in patients who require spine fusion.

Interventions

  • DEVICE OssDsign® Catalyst

Study Locations (13)

Connecticut

  • Orthopedic Associates of Hartford — Hartford
  • Central Connecticut Neurosurgery and Spine — New Britian
  • Yale Center for Clinical Investigation, Yale School of Medicine — New Haven

California

  • Community Health Partners Neuroscience — Fresno
  • San Diego Neurosurgery — San Diego

Florida

  • Minimally Invasive Spine Center of South Florida — Miami
  • Foundation for Orthopaedic Research and Education — Tampa

Georgia

  • Northeast Georgia Medical Center — Gainesville

Illinois

  • Carle Foundation Hospital, NeuroScience Institute — Urbana

Kentucky

  • Orthopaedic Institute of Western Kentucky — Paducah

Maryland

  • OrthoBethesda Research Foundation — Bethesda

Minnesota

  • Twin Cities Orthopedics — Edina

Trial Details

FieldValue
Enrollment Target 450 participants
Start Date 2022-03-23
Est. Completion 2027-04-01

Sponsor

OssDsign

29 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05329129

The ClinicalTrials.gov registry entry for NCT05329129 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 450 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is OssDsign, which has 29 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Degenerative Disc Disease appearing as the primary indexed condition, and to 1 intervention — of which OssDsign® Catalyst 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: NCT05329129 reports 13 study locations spanning 9 distinct geographic areas — top geographies include Connecticut, California, Florida. 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 NCT05329129 about?

NCT05329129 is a clinical study titled "OssDsign® Spine Registry Study ("Propel")". The purpose of this multi-center, prospective, observational registry is to gather information on the clinical outcomes and real-world use of commercially available bone graft substitutes manufactured by OssDsign® AB, in patients who require spine fusion.

What is the current status of trial NCT05329129?

This trial is currently recruiting. The enrollment target is 450 participants. The study started on 2022-03-23. Estimated completion is 2027-04-01.

What conditions does trial NCT05329129 study?

This clinical trial studies the following conditions: Degenerative Disc Disease, 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 NCT05329129?

The interventions under investigation include: OssDsign® Catalyst (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05329129?

This trial is sponsored by OssDsign, which has 29 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05329129 being conducted?

This trial has 13 study locations across California, Connecticut, Florida, Georgia, Illinois. 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