NL-OMON37488已完成不适用
A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurostimulator System for the Management of Chronic Intractable Pain - Performance of the Spinal Modulation Neurostimulator System
Spinal Modulation NV0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •1.Subject is at least 18 years old
- •2.Subject is able and willing to comply with the follow-up schedule and protocol
- •3.Chronic, intractable pain in the thoracic, lumbar, and/or sacral distribution(s) for at least 6 months
- •4.Failed conservative treatments for chronic pain including but not limited to pharmacological therapy, physical therapy and interventional pain procedures for chronic pain
- •5.Minimum baseline pain rating of 60 mm on the VAS in the primary region of pain
- •6.In the opinion of the investigator, the subject is psychologically appropriate for the implantation for an active implantable medical device
- •7.Subject is able to provide written informed consent
- •8.Subject speaks Dutch or English
排除标准
- •1.Female subject of childbearing potential is pregnant/nursing, plans to become pregnant or is unwilling to use approved birth control
- •2.Escalating or changing pain condition within the past month as evidenced by investigator examination
- •3.Subject has had corticosteroid therapy at an intended site of stimulation within the past 30 days
- •4.Subject has had radiofrequency treatment of an intended target DRG(s) within the past 3 months
- •5.Subject currently has an active implantable device including ICD, pacemaker, spinal cord stimulator or intrathecal drug pump
- •6.Subject has pain only or primarily within a cervical dermatomal distribution
- •7.Subject is unable to operate the device
- •8.Subjects with indwelling devices that may pose an increased risk of infection
- •9.Subjects currently has an active infection
- •10.Subject has, in the opinion of the investigator, a medical comorbidity that contraindicates placement of an active medical device
- •11.Subject has participated in another clinical investigation within 30 days
- •12.Subject has a coagulation disorder or uses anticoagulants that, in the opinion of the investigator, precludes participation
- •13.Subject has been diagnosed with cancer in the past 2 years
研究者
相似试验
招募中
4 期
Two different toric IOLs from 2 different companies will be implanted and their final visual outcomes will be compared.CTRI/2024/03/064570Biotech vision care pvt ltd
进行中(未招募)
不适用
The effect of HF10™ Therapy on opioid analgesic use for the treatment of chronic intractable low back and/or radicular leg paiChronic intractable low back and/or radicular leg painMusculoskeletal DiseasesISRCTN11735894evro Corp49
已完成
不适用
Post-market surveillance study to evaluate tolerability, acceptance, improvement in quality of life and the course of symptoms in patients suffering from an acute uncomplicated urinary tract infection and receiving supportive treatment with Femannose®N30.0N39.0Urinary tract infection, site not specifiedAcute cystitisDRKS00016632Cassella-med GmbH & Co. KG103
尚未招募
4 期
A post-marketing surveillance for the Evaluation of the safety of TGlobulin25 for the induction of immunosuppressive therapy in adult kidney transplant candidatesIRCT20201230049888N1Kawsar biotech company100
尚未招募
Unknown
Post-market study of Pipit-NC Balloon Dilatation CatheterCTRI/2023/08/056616Sahajanand Medical Technologies Ltd. (SMT)
