Lumbar Fusion With Nanotube Versus Titanium Cage

Part of paid clinical trials in Lexington, Kentucky.

Sponsor
Francis Farhadi
Study ID
NCT07777718
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Adaptix nanoPEEK Cage — DEVICE
    FDA- approved interbody cage used during lumbar fusion surgery.
  • Capstone PTC Cage — DEVICE
    FDA- approved interbody cage used during lumbar fusion surgery.

Study Details

This study is comparing two FDA-approved cages used during lower back surgery. The study will look at whether one cage helps the bones in the back fuse together better than the other. Adults who are having a 1 or 2 level lumbar fusion surgery will be randomly assigned to receive either the Adaptix nanoPEEK cage or the Capstone PTC cage. Participants will have follow-up visits with imaging and questionnaires to evaluate bone fusion, back and leg pain, physical function, and overall health.

Key Dates

First listed
Aug 20, 2026
Start date
Sep 30, 2026
Status verified
Aug 2026
Primary completion
Apr 30, 2028
Completion
Apr 30, 2028

Study Design

Enrollment
108 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Adaptix nanoPEEK Cage
    Participants will receive the Adaptix nanoPEEK Cage during lumbar fusion surgery.
  • Active Comparator: Capstone PTC Cage
    Participants will receive the Capstone PTC Cage during lumbar fusion surgery.

Primary Outcome Measure

Radiographic Fusion [ Time Frame: 6 Months After Surgery ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of KentuckyLexingtonKentucky40506
Francis Farhadi, MD, PhD
[email protected]
859-562-0247

Find similar trials in Lexington, KY

By research site
University of Kentucky· Lexington, KY

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