Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05583864 · ClinicalTrials.gov registry record · NA
Lumbar Fusion With Porous Versus Non-Porous Cages
A NA study of Spinal Fusion and Spondylolisthesis, sponsored by Francis Farhadi.
- Active
- Registry status
- NA
- Development phase
- 108
- Enrollment target
- 1
- Study location
NCT05583864: Active NA study of Spinal Fusion and Spondylolisthesis, sponsored by Francis Farhadi.
NCT05583864 is a NA study of Spinal Fusion and Spondylolisthesis that is active but no longer recruiting, run by Francis Farhadi. The registered enrollment target is 108 participants, below the 478-participant average among 19 other Spinal Fusion trials with a reported enrollment target (77% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05583864, a NA study of Spinal Fusion and Spondylolisthesis, is active but no longer recruiting, sponsored by Francis Farhadi.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 108 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this single site, randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo lumbar interbody fusion procedures (TLIF), supplemented with pedicle screw instrumentation, using one of the following interventions: 1. Porous titanium cages 2. Non-porous titanium-coated poly-ether-ether-ketone (PEEK) cages.
Primary Outcome
Graded radiographic evaluation of ossification and/or pseudarthrosis between vertebrae. The evaluation applies a three-level scale of fusion success: BSF-1: Radiographical pseudarthrosis BSF-2: Radiographical locked pseudarthrosis BSF-3: Radiographical fusion Radiographic Success: Radiographic success is defined by radiographical fusion (BSF-3) presenting bone bridges within at least half of the fusion area with at least the density originally achieved at surgery. Radiographic Failure: Radiog
Conditions Studied
Interventions
- DEVICE CONDUIT Porous Titanium Spinal Cage
- DEVICE PROTI 360 Titanium-Coated PEEK Spinal Cage
Study Locations (1)
Kentucky
- University of Kentucky - Lexington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 108 participants |
| Start Date | 2022-11-01 |
| Est. Completion | 2027-06 |
| Phase | NA |
What the registry record for NCT05583864 still lists
NCT05583864 is an interventional study that assigns participants to a tested intervention. The registered 108 participants enrollment target is mid-sized for trials with a published cap, below the 478-participant average among 19 other Spinal Fusion trials with a reported enrollment target (77% lower).
The record links to 5 conditions, with Spinal Fusion appearing as the primary indexed condition, and to 2 interventions - of which CONDUIT Porous Titanium Spinal Cage is the first listed.
NCT05583864 reports a single indexed study location in Kentucky.
Frequently Asked Questions
What is clinical trial NCT05583864 about?
NCT05583864 is a clinical study titled "Lumbar Fusion With Porous Versus Non-Porous Cages". The objective of this single site, randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo lumbar interbody fusion procedures (TLIF), supplemented with pedicle screw instrumentation, using one of the following interventions: 1. Porous t...
What is the current status of trial NCT05583864?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 108 participants. The study started on 2022-11-01. Estimated completion is 2027-06.
What conditions does trial NCT05583864 study?
This clinical trial studies the following conditions: Spinal Fusion, Spondylolisthesis, Arthrodesis, Lumbar Fusion, Pseudarthrosis.
What interventions are being tested in trial NCT05583864?
The interventions under investigation include: CONDUIT Porous Titanium Spinal Cage (DEVICE), PROTI 360 Titanium-Coated PEEK Spinal Cage (DEVICE).
Who is sponsoring clinical trial NCT05583864?
This trial is sponsored by Francis Farhadi, which has 8 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05583864 being conducted?
This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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 NCT05583864's enrollment target sits among peer trials
108 10th of 19 higher than 10 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
-
Pulse-Width Modulation
RECRUITING · NA
-
Photobiomodulation for Lower Back Pain Post Spinal Fusion and Decompression Surgery
RECRUITING · NA
-
Kids With Iron Deficiency and Scoliosis
RECRUITING · NA
-
Trans-Auricular Stimulation for Postoperative Inflammation in Spine Surgery
RECRUITING · NA
-
Postoperative Pain Control in AIS Using Liposomal Bupivacaine vs. 0.25% Bupivacaine With Epinephrine
RECRUITING · NA
-
Alvimopan and Ileus in PSF
COMPLETED · NA
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
- NCT02703207 · 108 participants · NA
Neurocognitive and Health Impact of Sleep Apnea in Elderly Veterans With Comorbid COPD
- NCT02744677 · 108 participants · NA
COMPASSION S3 - Evaluation of the SAPIEN 3 Transcatheter Heart Valve in Patients With Pulmonary Valve Dysfunction
- NCT02781883 · 108 participants · Phase 2
Clinical Trial of BP1001 in Combination With With Venetoclax Plus Decitabine in AML
- NCT03848663 · 108 participants · NA
Visual Remapping to Aid Reading With Field Loss
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