70. 広範脊柱管狭窄症 Spinal stenosis Clinical trials / Disease details


臨床試験数 : 95 薬物数 : 169 - (DrugBank : 61) / 標的遺伝子数 : 68 - 標的パスウェイ数 : 90

  
23 trials found
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1NCT05630404
(ClinicalTrials.gov)
November 28, 20221/11/2022Efficacy of Surgical Injection Lumbar Erector Spinae Plane BlockEfficacy of Surgical Injection Lumbar Erector Spinae Plane Block for Pain Management Following Lumbar Spinal Fusion SurgeryLumbar Spine Instability;Lumbar Spinal Stenosis;Lumbar Spine DegenerationDrug: Surgical ESPB;Drug: US guided ESPBBursa City HospitalNULLRecruiting18 Years65 YearsAll90N/ATurkey
2NCT05345249
(ClinicalTrials.gov)
June 1, 202228/3/2022Erector Spinae Plane Block as Pain Management After Lumbar Fusion SurgeryErector Spinae Plane Block for Reduction of Early Postoperative Pain Scores and Opioid Use in Lumbar Spinal Fusion Surgery, a Prospective Double-blinded Randomized Placebo-controlled TrialSpondylolisthesis;Lumbar Disc Herniation;Lumbar Spinal Stenosis;Lumbar Disc Disease;Lumbar Spondylolisthesis;Lumbar Spondylosis;Lumbar Spine Disease;Lumbar Radiculitis;Spinal Fusion;Fusion of Spine;Spondylosis Lumbosacral RegionDrug: Ropivacaine Hydrochloride Injection;Drug: Sodium chlorideMaaike FentenRadboud University Medical CenterRecruiting18 YearsN/AAll76Phase 4Netherlands
3ChiCTR2100053054
2021-11-092021-11-10Desomumab and lumbar spinal stenosisEvaluation of bone mineral density and function at 1 year after lumbar spinal stenosis and fusion with desomumab: a parallel double-blind randomized controlled clinical trial Lumber diseaseGroup A:Denosumab;Group B:Placebo;The First Affiliated Hospital (Shenzhen People's Hospital), Southern University of Science and TechnologyNULLRecruiting4090BothGroup A:40;Group B:40;Phase 4China
4NCT04483297
(ClinicalTrials.gov)
November 18, 202014/7/2020First-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 SurgeryDegenerative Spondylolisthesis;Spinal StenosisDrug: AK1320 MS;Other: ControlAsahi Kasei Pharma CorporationEmergent Clinical Consulting, LLCActive, not recruiting22 Years80 YearsAll40Phase 1Canada
5NCT04042948
(ClinicalTrials.gov)
June 24, 201913/7/2019Clinical Effect of Preventive Use of Tylenol on Fever After Removal of Drainage Tube in Lumbar Fusion SurgeryRandomized 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 FusionLumbar Spinal Stenosis;Lumbar Disc Herniation;Lumbar RadiculopathyDrug: TylenolPeking University Third HospitalNULLCompleted18 YearsN/AAll183N/AChina
6NCT04007094
(ClinicalTrials.gov)
February 12, 201924/4/2019Single-Armed Use of ViviGen Cellular Bone Matrix in Patients Undergoing Posterolateral Lumbar SurgeryA Prospective, Single Arm Study of Patients Undergoing Posterolateral Lumbar Fusion (Without Interbody) Supplemented With ViviGen Cellular Bone MatrixDegenerative Disc Disease;Spinal Stenosis;Spondylosis;SpondylolisthesisDrug: ViviGen Cellular Bone MatrixOhio State UniversityDePuy SynthesRecruiting18 YearsN/AAll50Phase 4United States
7NCT03745040
(ClinicalTrials.gov)
January 26, 20195/11/2018Liposomal Bupivacaine in One-level Instrumented Posterior Spinal FusionDoes Liposomal Bupivacaine Improve Postoperative Pain Control After One Level Posterior Spinal Fusion With InstrumentationLumbar Spinal Stenosis;Lumbar Disc Herniation;Lumbar Disc Disease;Lumbar SpondylolisthesisDrug: Liposomal bupivacaineAllina Health SystemTwin Cities Spine CenterRecruiting18 YearsN/AAll60Phase 4United States
8NCT03883022
(ClinicalTrials.gov)
September 3, 201810/3/2019Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine SurgeryVancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine SurgerySpinal Fusion;Spinal Stenosis;SpondylolisthesisDrug: with U-VANCO (vancomycin hydrochloride);Drug: without U-VANCO (vancomycin hydrochloride)Taipei Veterans General Hospital, TaiwanNULLRecruiting20 YearsN/AAll400N/ATaiwan
9ChiCTR1800016968
2018-07-152018-07-05A prospective study on the effect of different antiosteoporosis drugs on patients after lumbar fusion surgeryA prospective study on the effect of different antiosteoporosis drugs on patients after lumbar fusion surgery Osteoporosis with lumbar spinal stenosisC:Lumbar Fusion Surgery+Basic anti-osteoporosis drugs;A:Lumbar Fusion Surgery+MenatetrenoneSoft Capsules;B:Lumbar Fusion Surgery+Teriparatide acetate;Qilu Hospital of Shandong UniversityNULLRecruiting2080BothC:40;A:40;B:40;China
10EUCTR2016-002887-14-FI
(EUCTR)
31/10/201614/10/2016Dose-response of ketamine in patient controlled analgesia in orthopaedic surgery patientsDose response study of Patient Controlled Analgesia (PCA) of S-ketamine in orthopaedic spine surgery patients - DoseRespKeta Patients who are scheduled for elective posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation
MedDRA version: 19.0;Level: LLT;Classification code 10041595;Term: Spinal stenosis lumbar;System Organ Class: 100000004859;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11]
Trade Name: Ketanest-S
INN or Proposed INN: KETAMINE
Trade Name: Oxycodone Orion
INN or Proposed INN: OXYCODONE
University of TurkuNULLNot RecruitingFemale: yes
Male: yes
100Phase 1;Phase 4Finland
11NCT02700451
(ClinicalTrials.gov)
March 201618/2/2016Post-op Acetaminophen vs NSAID Use on Lumbar Spinal Fusion OutcomesA Randomized Controlled Trial of Post-operative Acetaminophen Versus Nonsteroidal Anti-Inflammatory Drug (NSAID) Use on Lumbar Spinal Fusion OutcomesLumbar Osteoarthritis;Spondylosis;Lumbar Disc Disease;Spinal StenosisDrug: Ketorolac;Drug: Acetaminophen;Drug: PlaceboHospital for Special Surgery, New YorkNULLActive, not recruiting18 Years75 YearsAll300N/AUnited States
12EUCTR2014-003252-31-FI
(EUCTR)
15/05/201522/04/2015Dose-response of dexmedetomidine in patient controlled analgesia in orthopaedic surgery patientsDose response study of Patient Controlled Analgesia (PCA) of Dexmedetomidine in orthopaedic spine surgery patients - DoserespDex_2.0 Patients, who are scheduled for elective posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation
MedDRA version: 17.1;Level: LLT;Classification code 10041595;Term: Spinal stenosis lumbar;System Organ Class: 100000004859;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11]
Trade Name: Dexdor
INN or Proposed INN: deksmedetomidiini
Other descriptive name: DEXMEDETOMIDINE HYDROCHLORIDE
Trade Name: Oxanest
INN or Proposed INN: oksikodoni
Other descriptive name: OXYCODONE HYDROCHLORIDE
University of TurkuNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
Finland
13NCT02070484
(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
14NCT02090244
(ClinicalTrials.gov)
August 201216/3/2014Does PTH 1-34 (Teriparatide) Enhance Spinal Fusion in Humans?Förbättrar PTH Postero-lateral fusionsläkning Vid Ryggkirurgi?Spinal StenosisDrug: TeriparatideUniversity Hospital, LinkoepingMedical Research Council of Southeast SwedenCompletedN/AN/AAll34Phase 4Sweden
15EUCTR2011-006152-36-DK
(EUCTR)
10/05/201210/05/2012Does postoperative treatment with parathyroidea hormone Forteo®improve the disability inelderly patients undergoing spinal stabilization fusion surgery comparedwith patients treated with placebo. If that is the case, is there a correlationbetween improvement of disability and solid osseous healing?Postoperative treatment with parathyroidea hormone Forteo® inpatients undergoing posterolateral spinal fusion surgery. A prospektiveand a randomized double-blinded, placebo-controlled study - PTH-U-DESE-STUDY Spinal stenosis
MedDRA version: 14.1;Level: LLT;Classification code 10041597;Term: Spinal stenosis of lumbar region;System Organ Class: 10028395 - Musculoskeletal and connective tissue disorders;Therapeutic area: Diseases [C] - Musculoskeletal Diseases [C05]
Trade Name: Forteo
Product Name: Forsteo
Product Code: 0002-8971
INN or Proposed INN: teriparatide [rDNA origin] contains recombinant human parathyroid hormone (1-34)
Other descriptive name: rhPTH (1-34)
Middelfart RygsektorNULLNot RecruitingFemale: yes
Male: yes
100Phase 2Denmark
16EUCTR2011-002917-12-SE
(EUCTR)
06/12/201127/09/2011Does parathyroid hormone enhance healing after spinal fusion?Does PTH enhance healing after spinal fusion? - PTH spinal stenosis Decompression and fusion due to spinal stenosis in men and postmenopausal women. In this study we want to examine if Forsteo (teriparatide) improves bone healing (jugded by blinded investigators) and if this improves the function and decreases the pain at 7 weeks and 6 months.;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11]Trade Name: ForsteoDepartment of Orthopaedics IKEDepartment of Orthopaedics IKENot RecruitingFemale: yes
Male: yes
100Phase 4Sweden
17NCT01377623
(ClinicalTrials.gov)
September 20103/1/2011Pilot Study on the Effect of Dexmedetomidine on Inflammatory Responses in Patients Undergoing Lumbar Spinal FusionPilot Study on the Effect of Dexmedetomidine on Inflammatory Responses in Patients Undergoing Lumbar Spinal FusionSpinal Stenosis;InflammationDrug: Dexmedetomidine group;Drug: Placebo groupNew York University School of MedicineHospira, now a wholly owned subsidiary of PfizerTerminated18 YearsN/AAll66N/AUnited States
18NCT01097486
(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
19NCT01106417
(ClinicalTrials.gov)
June 201016/4/2010Safety and Efficacy Study of NeoFuse in Subjects Undergoing Multi-Level Anterior Cervical Discectomy and FusionPhase 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;Device: MasterGraft GranulesMesoblast, Ltd.NULLCompleted18 Years70 YearsAll12Phase 1/Phase 2Australia
20NCT00996073
(ClinicalTrials.gov)
September 20099/10/2009Safety and Preliminary Efficacy Study of NeoFuse in Subjects Requiring Lumbar Interbody FusionA Prospective, Multicenter, Randomized, Open-Label, Controlled Study Evaluating Safety and Preliminary Efficacy of NeoFuse When Combined With MasterGraft Matrix in Subjects Undergoing Lumbar Interbody Fusion With InstrumentationDegenerative Disc Disease;Degenerative Spondylolisthesis;Spinal StenosisBiological: Lumbar Interbody Fusion with Autograft;Biological: Lumbar Interbody Fusion with NeoFuseMesoblast, Ltd.NULLCompleted18 Years70 YearsAll24Phase 2United States
21NCT00808665
(ClinicalTrials.gov)
June 200915/12/2008Intraoperative Infusion of Precedex to Reduce Length of Stay After Lumbar Spine FusionDoes Continuous Perioperative Dexmedetomidine Infusion Reduce Time to Discharge in Patients Undergoing Major Lumbar Fusion? A Double-Blind, Placebo-Controlled StudySpinal Fusion Acquired;Spinal Stenosis;Lesions of Lumbosacral Intervertebral Disc;Spinal DiseasesDrug: Dexmedetomidine;Drug: 0.9% SalineVanderbilt University Medical CenterNULLCompleted18 Years85 YearsAll68Phase 4United States
22NCT00810212
(ClinicalTrials.gov)
November 200817/12/2008Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar FusionA Prospective, Multicenter, Randomized, Open-Label, Controlled Study Evaluating Safety and Preliminary Efficacy of NeoFuse When Combined With Mastergraft Granules in Subjects Undergoing Posterolateral Lumbar Fusion With InstrumentationDegenerative Disc Disease;Degenerative Spondylolisthesis;Spinal StenosisProcedure: PLF with autograft;Biological: PLF with NeoFuseMesoblast, Ltd.NULLWithdrawn18 Years70 YearsAll0Phase 1/Phase 2United States
23NCT00549913
(ClinicalTrials.gov)
October 200724/10/2007Study of 3 Doses of NeoFuse Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion (PLF)A Dose-escalation Study to Assess the Feasibility and Safety of 3 Different Doses of NeoFuse When Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion With Instrumentation.Degenerative Disc Disease;Spondylolisthesis;Spinal StenosisBiological: NeoFuse;Procedure: posterolateral spinal fusion with instrumentationMesoblast, Ltd.NULLCompleted18 YearsN/AAll6Phase 1/Phase 2United States