Elite in Spinal Fusion

Dr. Pierce D. Nunley

Orthopedics
Spine Institute Of Louisiana LLC
1500 Line Ave, Suite 200, 
Shreveport, LA 
Clinical Trials:Currently Recruiting for 1 Trial
Accepting New Patients
Elite in Spinal Fusion
Spine Institute Of Louisiana LLC
1500 Line Ave, Suite 200, 
Shreveport, LA 
OverviewInsuranceLocationsClinical Research

Overview

Pierce Nunley is an Orthopedics provider in Shreveport, Louisiana. Dr. Nunley is rated as an Elite provider by MediFind in Spinal Fusion. His top areas of expertise are Invertebral Disc Disease, Lordosis, Cervical Spondylosis, Spinal Fusion, and Osteotomy. Dr. Nunley is currently accepting new patients.

His clinical research consists of co-authoring 126 peer reviewed articles and participating in 10 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 52 articles in the study of Spinal Fusion.

Specialties
Orthopedics
Licenses
Orthopaedic Surgery in LA
Hospital Affiliations
Springhill Medical Center
Specialists Hospital Shreveport
Christus St Michael Health System
Willis Knighton Medical Center
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
  • POS
  • PPO
Anthem
  • EPO
  • HMO
  • POS
  • PPO
Blue Cross Blue Shield
  • EPO
  • HMO
  • POS
  • PPO
Cigna
  • EPO
  • HMO
  • PPO
Health Care Services Corporation
  • HMO
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • MEDICARE SNP
  • OTHER COMMERCIAL
  • OTHER MEDICARE
  • OTHER MEDICARE PART D
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Louisiana Healthcare Connections
  • HMO
  • MANAGED MEDICAID PLAN
Medicaid
  • OTHER MEDICAID
  • STATE MEDICAID
UnitedHealthcare
  • EPO
  • HMO
  • POS
  • PPO
Wellcare
  • EPO
  • HMO
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • MEDICARE SNP
  • MEDICARE-MEDICAID PLAN
  • OTHER MEDICARE
  • OTHER MEDICARE PART D
View 5 Less Insurance Carriers -

Locations

SPINE INSTITUTE OF LOUISIANA LLC
1500 Line Ave, Suite 200, Shreveport, LA 71101

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

10 Clinical Trials

A 2 and 5 Year Evaluation of Clinical Outcomes in the Treatment of Degenerative Spinal Stenosis With Concomitant Low Back Pain by Decompression With Additional Stabilization Using the Coflex® Interlaminar Technology for FDA Actual Conditions for Use Study.
A 2 and 5 Year Evaluation of Clinical Outcomes in the Treatment of Degenerative Spinal Stenosis With Concomitant Low Back Pain by Decompression With Additional Stabilization Using the Coflex® Interlaminar Technology for FDA Actual Conditions for Use Study.
Enrollment Status: Recruiting
Publish Date: January 05, 2024
Intervention Type: Procedure, Device
Study Phase: Not Applicable
A Multi-Center, Prospective, Randomized Controlled Trial Comparing the Safety and Effectiveness of Prodisc® C SK and Prodisc® C Vivo to Mobi-C® Cervical Disc in the Treatment of Two-Level Symptomatic Cervical Disc Disease (SCDD)
A Multi-Center, Prospective, Randomized Controlled Trial Comparing the Safety and Effectiveness of Prodisc® C SK and Prodisc® C Vivo to Mobi-C® Cervical Disc in the Treatment of Two-Level Symptomatic Cervical Disc Disease (SCDD)
Enrollment Status: Active_not_recruiting
Publish Date: July 30, 2025
Intervention Type: Device
Study Phase: Not Applicable
Multi Center, Prospective Evaluation for Clinical and Radiographic Outcomes Utilizing Stryker Spine Cervical and Lumbar Interbody Systems: Observational Post Market Clinical Follow up Study
Multi Center, Prospective Evaluation for Clinical and Radiographic Outcomes Utilizing Stryker Spine Cervical and Lumbar Interbody Systems: Observational Post Market Clinical Follow up Study
Enrollment Status: Terminated
Publish Date: April 18, 2025
Intervention Type: Device
A Prospective Data Collection Study of Patients Treated With a Single-Level Lumbar Interbody Fusion Stabilized With Pedicle Screws
A Prospective Data Collection Study of Patients Treated With a Single-Level Lumbar Interbody Fusion Stabilized With Pedicle Screws
Enrollment Status: Active_not_recruiting
Publish Date: March 26, 2025
Intervention Type: Procedure
Rampart Duo Clinical (RaDical) Study: An Exempt Minimal Risk Post-Market Evaluation of Clinical Outcomes
Rampart Duo Clinical (RaDical) Study: An Exempt Minimal Risk Post-Market Evaluation of Clinical Outcomes
Enrollment Status: Completed
Publish Date: December 01, 2023
Intervention Type: Other
Prospective Evaluation Of Lumbar Discectomy With Additional Implantation Of An Annular Closure Device In Patients With Large Postsurgical Annular Defects For Prevention Of Lumbar Disc Reherniation
Prospective Evaluation Of Lumbar Discectomy With Additional Implantation Of An Annular Closure Device In Patients With Large Postsurgical Annular Defects For Prevention Of Lumbar Disc Reherniation
Enrollment Status: Unknown
Publish Date: September 28, 2023
Intervention Type: Device
Study Phase: Not Applicable
A Prospective, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of a Single Injection of Rexlemestrocel-L Alone or Combined With Hyaluronic Acid (HA) in Subjects With Chronic Low Back Pain
A Prospective, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of a Single Injection of Rexlemestrocel-L Alone or Combined With Hyaluronic Acid (HA) in Subjects With Chronic Low Back Pain
Enrollment Status: Completed
Publish Date: October 19, 2022
Intervention Type: Drug
Study Drugs: Rexlemestrocel-L, Rexlemestrocel-L+Hyaluronic Acid
Study Phase: Phase 3
Spineology Clinical Outcomes Trial: An Investigation Device Exempt (IDE) Performance Goal Clinical Investigation
Spineology Clinical Outcomes Trial: An Investigation Device Exempt (IDE) Performance Goal Clinical Investigation
Enrollment Status: Completed
Publish Date: October 20, 2021
Intervention Type: Device
Study Phase: Not Applicable
A Single-arm, Prospective, Multi-center Study of Nucel® in Patients Receiving Interbody Fusion for One and Two Level Degenerative Disease of the Lumbar Spine
A Single-arm, Prospective, Multi-center Study of Nucel® in Patients Receiving Interbody Fusion for One and Two Level Degenerative Disease of the Lumbar Spine
Enrollment Status: Unknown
Publish Date: May 26, 2021
Intervention Type: Other, Procedure
Study Phase: Not Applicable
A 2 and 5 Year Comparative Evaluation of Clinical Outcomes in the Treatment of Moderate Lumbar Spinal Stenosis With the Superion® Indirect Decompression System (IDS) vs. Direct Decompression Surgery for FDA Actual Conditions of Use Study
A 2 and 5 Year Comparative Evaluation of Clinical Outcomes in the Treatment of Moderate Lumbar Spinal Stenosis With the Superion® Indirect Decompression System (IDS) vs. Direct Decompression Surgery for FDA Actual Conditions of Use Study
Enrollment Status: Withdrawn
Publish Date: June 12, 2019
Intervention Type: Procedure, Device
Study Phase: Not Applicable
View 9 Less Clinical Trials

126 Total Publications

Beyond Pain Relief: Preventing Recurrence and Preserving Function After Lumbar Discectomy.
Beyond Pain Relief: Preventing Recurrence and Preserving Function After Lumbar Discectomy.
Journal: International journal of spine surgery
Published: October 14, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

Learn more about MediFind’s expert tiers

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