- 10995 Quivira Road, Overland Park, Kansas 66210, United States
- Mon - Fri 8am - 5pm
BENEFIT– Prospective, multi-center, randomized, parallel assignment, single-blind, interventional feasibility study. Prospective Clinical Trial of Duty Cycled Stimulation Using the Senza™ Spinal Cord Stimulation (SCS) System: CA2015OUS DC.
A Prospective, Multi-Center, Bi-Phasic Randomized Design to Compare Outcomes of the CornerLoc™ SI Joint Stabilization System and Intra-Articular Sacroiliac Joint Steroid Injection in Patients with Refractory Sacroiliac Joint Dysfunction
A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group, Multicenter Study to Evaluate the Safety and Efficacy of SP-103 in Subjects with Moderate to Severe Acute Lower Back Pain
Open-Label, Post Market Study: A Clinical Trial to Study the Effects of DTM Spinal Cord Stimulation (DTM™SCS) programs in treating Intractable Chronic Back Pain in Subjects without prior history of Spine Surgery
A Post-Market, Observational Clinical Study to Evaluate the Effects of DTMTM SCS programming in treating Intractable Chronic Upper Extremity Limb Pain
SENZA-CAP – A Prospective Clinical Trial to Assess the Feasibility of the SenzaTM Spinal Cord Stimulation (SCS) System in the Treatment of Chronic Abdominal Pain.
RELIEF – A Global Registry to Evaluate Long-Term Effectiveness of Neurostimulation Therapy for Pain.
Postmarket Registry for Evaluation of the Superion® Spacer.
A randomized, double-blind, placebo-controlled, Phase III trial to evaluate the efficacy and safety of a single intra-articular injection of RTX-GRT7039 in adult subjects with pain associated with osteoarthritis of the knee
A Phase 3, Multicenter, Randomized, Open-Label Study to Evaluate the Long-Term Safety and Tolerability Of Oral Atogepant For the Prevention Of Migraine In Participants With Episodic Migraine
The UPGRADE Study: Real World Outcomes® of Differential Target Multiplexed (DTM-SCS®) Stimulation in Existing and New Medtronic Intellis™ Implants
Spinal Cord Stimulation in the treatment of Chronic, Intractable Pain using the Nalu™ Neurostimulation System (nPower™-US)
Treatment of Post-Operative Pain Following Orthopedic Surgery with SPRINT® Peripheral Nerve Stimulation (PNS) System in a Randomized, Double-Blinded, Placebo-Controlled Study.
A Randomized, Double-blind, Placebo-Controlled, Pilot Study to Evaluate the Safety and Effectiveness of LUCEMYRA in the Treatment of Opioid Withdrawal During an Opioid Taper in Subjects with Chronic Non-Cancer Pain
A Multicenter, Randomized, Double-blind, Sham Controlled, Comparative Study of SI-6603 in Subjects with Lumbar Disc Herniation (Phase 3)
AXS-07-301: MOMENTUM (Maximizing Outcomes in Treating Acute Migraine): A Randomized, Double-blind, Single-dose, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-07 (meloxicam and rizatriptan) for the Acute Treatment of Migraine in Adults with Inadequate Response to Prior Acute Treatments
Primary objective:
A Prospective, Multicenter, Randomized, Double-Blinded, Sham-Controlled Study to Evaluate the Efficacy and Safety of Clonidine Micropellets for the treatment of Pain Associated with Lumbosacral Radiculopathy in Adults: RePRIEVE-CM (achieving Radicular Pain Relief Via Epidural injection of Clonidine Micropellets). STX-015-18-01.
A Multicenter, Randomized, Follow-up Study to Evaluate the Long-Term Safety of Clonidine Micropellets for the Treatment of Pain Associated with Lumbosacral Radiculopathy in Adults: RePRIEVE-CM-LT (achieving Radicular Pain RelIEf Via Epidural injection of Clonidine Micropellets Long-Term) STX-015-18-02
BENEFIT– Prospective, multi-center, randomized, parallel assignment, single-blind, interventional feasibility study. Prospective Clinical Trial of Duty Cycled Stimulation Using the Senza™ Spinal Cord Stimulation (SCS) System: CA2015OUS DC.
A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group, Multicenter Study to Evaluate the Safety and Efficacy of SP-103 in Subjects with Moderate to Severe Acute Lower Back Pain
A Post-Market, Observational Clinical Study to Evaluate the Effects of DTMTM SCS programming in treating Intractable Chronic Upper Extremity Limb Pain
RELIEF – A Global Registry to Evaluate Long-Term Effectiveness of Neurostimulation Therapy for Pain.
A randomized, double-blind, placebo-controlled, Phase III trial to evaluate the efficacy and safety of a single intra-articular injection of RTX-GRT7039 in adult subjects with pain associated with osteoarthritis of the knee
The UPGRADE Study: Real World Outcomes® of Differential Target Multiplexed (DTM-SCS®) Stimulation in Existing and New Medtronic Intellis™ Implants
Treatment of Post-Operative Pain Following Orthopedic Surgery with SPRINT® Peripheral Nerve Stimulation (PNS) System in a Randomized, Double-Blinded, Placebo-Controlled Study.
A Multicenter, Randomized, Double-blind, Sham Controlled, Comparative Study of SI-6603 in Subjects with Lumbar Disc Herniation (Phase 3)
AXS-07-301: MOMENTUM (Maximizing Outcomes in Treating Acute Migraine): A Randomized, Double-blind, Single-dose, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-07 (meloxicam and rizatriptan) for the Acute Treatment of Migraine in Adults with Inadequate Response to Prior Acute Treatments
A Prospective, Multi-Center, Bi-Phasic Randomized Design to Compare Outcomes of the CornerLoc™ SI Joint Stabilization System and Intra-Articular Sacroiliac Joint Steroid Injection in Patients with Refractory Sacroiliac Joint Dysfunction
Open-Label, Post Market Study: A Clinical Trial to Study the Effects of DTM Spinal Cord Stimulation (DTM™SCS) programs in treating Intractable Chronic Back Pain in Subjects without prior history of Spine Surgery
SENZA-CAP – A Prospective Clinical Trial to Assess the Feasibility of the SenzaTM Spinal Cord Stimulation (SCS) System in the Treatment of Chronic Abdominal Pain.
Postmarket Registry for Evaluation of the Superion® Spacer.
A Phase 3, Multicenter, Randomized, Open-Label Study to Evaluate the Long-Term Safety and Tolerability Of Oral Atogepant For the Prevention Of Migraine In Participants With Episodic Migraine
Spinal Cord Stimulation in the treatment of Chronic, Intractable Pain using the Nalu™ Neurostimulation System (nPower™-US)
A Randomized, Double-blind, Placebo-Controlled, Pilot Study to Evaluate the Safety and Effectiveness of LUCEMYRA in the Treatment of Opioid Withdrawal During an Opioid Taper in Subjects with Chronic Non-Cancer Pain
A Prospective, Multicenter, Randomized, Double-Blinded, Sham-Controlled Study to Evaluate the Efficacy and Safety of Clonidine Micropellets for the treatment of Pain Associated with Lumbosacral Radiculopathy in Adults: RePRIEVE-CM (achieving Radicular Pain Relief Via Epidural injection of Clonidine Micropellets). STX-015-18-01.
A Multicenter, Randomized, Follow-up Study to Evaluate the Long-Term Safety of Clonidine Micropellets for the Treatment of Pain Associated with Lumbosacral Radiculopathy in Adults: RePRIEVE-CM-LT (achieving Radicular Pain RelIEf Via Epidural injection of Clonidine Micropellets Long-Term) STX-015-18-02
We love our patients, so feel free to call during normal business hours and ask about current trials.
Overland Park, Kansas - (Kansas City area)
10995 Quivira Road, Overland Park, Kansas 66210, United States