70. Spinal stenosis Clinical trials / Disease details


Clinical trials : 96 Drugs : 203 - (DrugBank : 60) / Drug target genes : 66 - Drug target pathways : 89

  
4 trials found
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agemin
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PhaseCountries
1NCT04537026
(ClinicalTrials.gov)
June 16, 202128/8/2020The SAFE Trial. Sterile Amniotic Fluid Filtrate Epidural Injection.A Phase I/II Double-Blinded Randomized Prospective Study of Sterile Amniotic Fluid Filtrate Epidural Injection for the Treatment of Lumbosacral Radicular Pain Due to Spinal Stenosis: The SAFE Trial (Improving Safety and Outcomes in the Treatment of Pain and Disability Related to Spinal Stenosis).Lumbar Spinal StenosisDrug: Amniotic Fluid Allograft;Drug: Dexamethasone sodium phosphateUniversity of UtahCell Therapy & Regenerative Medicine;SKAGGs FoundationRecruiting18 YearsN/AAll112Phase 1/Phase 2United States
2NCT02070484
(ClinicalTrials.gov)
February 201421/2/2014Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc DiseaseEfficacy of a Human Amniotic Tissue-derived Allograft, NuCel, in Patients Undergoing Posteriolateral Lumbar Fusions for Degenerative Disc DiseaseLumbar Degenerative Disc Disease;Spinal Stenosis;Spondylolisthesis;Spondylosis;Intervertebral Disk Displacement;Intervertebral Disk Degeneration;Spinal Diseases;Bone Diseases;Musculoskeletal Diseases;SpondylolysisBiological: NuCel;Biological: Demineralized Bone MatrixOhioHealthNuTech Medical, IncTerminated18 Years75 YearsAll6N/AUnited States
3NCT01618435
(ClinicalTrials.gov)
March 20128/5/2012The Clinical Effect of i-FACTOR® Versus Allograft in Non-instrumented Posterolateral Spondylodesis Operation in the Elderly With Spinal Stenosis Due to Degenerative SpondylolisthesisThe Clinical Effect of i-FACTOR® Versus Allograft in Non-instrumented Posterolateral Spondylodesis OperationSpinal StenosisBiological: i-FACTORSygehus LillebaeltCeraPedics, IncActive, not recruiting60 YearsN/ABoth108Phase 3Denmark
4NCT01097486
(ClinicalTrials.gov)
June 201030/3/2010Safety and Preliminary Efficacy Study of NeoFuse in Subjects Undergoing Multi-Level Anterior Cervical DiscectomyPhase 2 Study Evaluating Safety and Preliminary Efficacy of NeoFuse When Combined With MasterGraft Matrix in Subjects Undergoing Multi-Level Anterior Cervical Discectomy and Fusion With Anterior Cervical Plate FixationCervical Degenerative Disc Disease;Degenerative Spondylolisthesis;Spinal StenosisBiological: NeoFuse;Procedure: AllograftMesoblast, Ltd.NULLCompleted18 Years70 YearsAll24Phase 2United States