70. 広範脊柱管狭窄症 Spinal stenosis Clinical trials / Disease details
臨床試験数 : 96 / 薬物数 : 203 - (DrugBank : 60) / 標的遺伝子数 : 66 - 標的パスウェイ数 : 89
Showing 1 to 10 of 27 diseases
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
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1 | NCT05023733 (ClinicalTrials.gov) | October 1, 2021 | 16/8/2021 | Clinical and Radiographic Outcomes of TLIF w/3D Printed Cellular Implant | Clinical and Radiographic Outcomes of Transforaminal Lumbar Interbody Fusion (TLIF) With a Novel 3D Printed Cellular Titanium Implant Clinical and Radiographic Outcomes of Transforaminal Lumbar Interbody Fusion(TLIF) With a Novel 3D P ... | Foraminal Stenosis;Degenerative Disc Disease;Lumbar Spondylolisthesis;Lumbar Spinal Stenosis | Device: CONDUIT™ Interbody Platform composed of the EIT (Emerging Implant Technologies) Cellular Titanium® Device: CONDUIT™ Interbody Platform composed of the EIT (Emerging Implant Technologies) Cellular Tit ... | Farhan Karim | DePuy Synthes | Not yet recruiting | 35 Years | 80 Years | All | 150 | United States | |
2 | NCT04483297 (ClinicalTrials.gov) | November 18, 2020 | 14/7/2020 | First-In-Human Study of AK1320 Encapsulated Microspheres (AK1320 MS) | First-In-Human Study of AK1320 Encapsulated Microspheres (AK1320 MS) In Subjects With Degenerative Spondylolisthesis and Concomitant Symptomatic Spinal Stenosis Who Are Undergoing Decompression And Single Level Instrumented Posterolateral Lumbar Autograft Fusion Surgery First-In-Human Study of AK1320 Encapsulated Microspheres (AK1320 MS) In Subjects With Degenerative S ... | Degenerative Spondylolisthesis;Spinal Stenosis | Drug: AK1320 MS;Other: Control | Asahi Kasei Pharma Corporation | Emergent Clinical Consulting, LLC | Recruiting | 22 Years | 80 Years | All | 40 | Phase 1 | Canada |
3 | NCT04308122 (ClinicalTrials.gov) | October 1, 2020 | 6/3/2020 | Cervical Orthosis Versus no Orthosis Following Multi-level Posterior Cervical Fusion | A Randomized Trial of Cervical Orthosis Versus no Orthosis Following Multi-level Posterior Cervical Fusion A Randomized Trial of Cervical Orthosis Versus no Orthosis Following Multi-level Posterior Cervical ... | Posterior Cervical Spinal Surgery;Myelopathy Cervical;Radiculopathy, Cervical;Spinal Stenosis Cervical;Spondylosis, Cervical Posterior Cervical Spinal Surgery;Myelopathy Cervical;Radiculopathy, Cervical;Spinal Stenosis Cervic ... | Device: Cervical Orthosis (CO);Device: No Orthosis | Dr. Christopher Bailey | NULL | Recruiting | 18 Years | N/A | All | 40 | N/A | Canada |
4 | NCT04379921 (ClinicalTrials.gov) | September 1, 2020 | 30/4/2020 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using the Apple Watch | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using the Apple Watch | Spine Disease;Spine Degeneration;Spinal Stenosis;Surgery;Spine Fusion | Device: Apple Watch and App | Stanford University | Stryker Nordic | Recruiting | 18 Years | N/A | All | 200 | N/A | United States |
5 | NCT04042948 (ClinicalTrials.gov) | June 24, 2019 | 13/7/2019 | Clinical Effect of Preventive Use of Tylenol on Fever After Removal of Drainage Tube in Lumbar Fusion Surgery Clinical Effect of Preventive Use of Tylenol on Fever After Removal of Drainage Tube in Lumbar Fusio ... | Randomized Controlled Study of Fever Probability, Risk Factors and Preventive Use of Non-steroidal Anti-inflammatory Drugs on Fever After Removal of Drainage Tube After Lumbar Fusion Randomized Controlled Study of Fever Probability, Risk Factors and Preventive Use of Non-steroidal A ... | Lumbar Spinal Stenosis;Lumbar Disc Herniation;Lumbar Radiculopathy | Drug: Tylenol | Peking University Third Hospital | NULL | Completed | 18 Years | N/A | All | 183 | N/A | China |
6 | NCT04007094 (ClinicalTrials.gov) | February 12, 2019 | 24/4/2019 | Single-Armed Use of ViviGen Cellular Bone Matrix in Patients Undergoing Posterolateral Lumbar Surgery Single-Armed Use of ViviGen Cellular Bone Matrix in Patients Undergoing Posterolateral Lumbar Surger ... | A Prospective, Single Arm Study of Patients Undergoing Posterolateral Lumbar Fusion (Without Interbody) Supplemented With ViviGen Cellular Bone Matrix A Prospective, Single Arm Study of Patients Undergoing Posterolateral Lumbar Fusion(Without Interbod ... | Degenerative Disc Disease;Spinal Stenosis;Spondylosis;Spondylolisthesis | Drug: ViviGen Cellular Bone Matrix | Ohio State University | DePuy Synthes | Recruiting | 18 Years | N/A | All | 50 | Phase 4 | United States |
7 | NCT03745040 (ClinicalTrials.gov) | January 26, 2019 | 5/11/2018 | Liposomal Bupivacaine in One-level Instrumented Posterior Spinal Fusion | Does Liposomal Bupivacaine Improve Postoperative Pain Control After One Level Posterior Spinal Fusion With Instrumentation Does Liposomal Bupivacaine Improve Postoperative Pain Control After One Level Posterior Spinal Fusio ... | Lumbar Spinal Stenosis;Lumbar Disc Herniation;Lumbar Disc Disease;Lumbar Spondylolisthesis | Drug: Liposomal bupivacaine | Allina Health System | Twin Cities Spine Center | Recruiting | 18 Years | N/A | All | 60 | Phase 4 | United States |
8 | NCT03883022 (ClinicalTrials.gov) | September 3, 2018 | 10/3/2019 | Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection f ... | Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection f ... | Spinal Fusion;Spinal Stenosis;Spondylolisthesis | Drug: with U-VANCO (vancomycin hydrochloride);Drug: without U-VANCO (vancomycin hydrochloride) | Taipei Veterans General Hospital, Taiwan | NULL | Recruiting | 20 Years | N/A | All | 400 | N/A | Taiwan |
9 | NCT03647501 (ClinicalTrials.gov) | August 22, 2018 | 21/8/2018 | Lumbar Fusion With Nexxt Spine 3D-Printed Titanium Interbody Cages | Lumbar Fusion With 3D-Printed Porous Titanium Interbody Cages - A Single-Blinded Randomized Controlled Trial Evaluating Nexxt Matrixx(TM) Versus PEEK Cages Lumbar FusionWith 3D-Printed Porous Titanium Interbody Cages - A Single-Blinded Randomized Controlle ... | Lumbar Degenerative Disc Disease;Lumbar Spinal Stenosis;Lumbar Spondylolisthesis;Lumbar Spinal Deformity;Lumbar Spondylosis Lumbar Degenerative Disc Disease;Lumbar Spinal Stenosis;Lumbar Spondylolisthesis;Lumbar Spinal Defor ... | Device: Interbody cage (titanium);Device: Interbody cage (PEEK) | Ohio State University | Nexxt Spine, LLC | Recruiting | 18 Years | N/A | All | 70 | N/A | United States |
10 | ChiCTR1800016968 | 2018-07-15 | 2018-07-05 | A prospective study on the effect of different antiosteoporosis drugs on patients after lumbar fusion surgery A prospective study on the effect of different antiosteoporosis drugs on patients after lumbar fusio ... | A prospective study on the effect of different antiosteoporosis drugs on patients after lumbar fusion surgery A prospective study on the effect of different antiosteoporosis drugs on patients after lumbar fusio ... | Osteoporosis with lumbar spinal stenosis | C:Lumbar Fusion Surgery+Basic anti-osteoporosis drugs;A:Lumbar Fusion Surgery+MenatetrenoneSoft Capsules;B:Lumbar Fusion Surgery+Teriparatide acetate; C:Lumbar FusionSurgery+Basic anti-osteoporosis drugs;A:Lumbar FusionSurgery+MenatetrenoneSoft Capsul ... | Qilu Hospital of Shandong University | NULL | Recruiting | 20 | 80 | Both | C:40;A:40;B:40; | China |