DRKS00020523已完成不适用
Post-Market Clinical Follow-up (PMCF) Study with the MOBIS II ST cage-implant for transforaminal lumbar fusion (TLIF) - PMCF MOBIS II ST
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 57
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 Years 至 one(—)
- 性别
- All
入选标准
- •Patients who are implanted routinely and in accordance with the certification of MOBIS II ST
排除标准
- •- Pregnant and breastfeeding women
- •- Patients incapable of giving consent
- •- Younger than 18 years old
- •- Patients without informed consent
研究者
相似试验
进行中(未招募)
不适用
A study to assess the safety and efficacy of hyaluronic acid dermal fillers in the treatment of facial agingISRCTN17960592Sinclair Pharmaceuticals Limited168
进行中(未招募)
3 期
A post-market clinical follow-up study of Perfectha Subskin LidocaineA range of Fitzpatrick skin types presenting significant loss of volume in the cheeks, jawline and/or chinSkin and Connective Tissue DiseasesISRCTN63865080Sinclair Pharma69
招募中
4 期
To study the effectiveness of surgical treatment in patients with knee joint paiCTRI/2023/12/060753Auxein Medical Pvt Ltd
已完成
不适用
Post-market clinical follow-up (PMCF) study to investigate the percentage of relapses in treatment with KadeFungin® Milchsäurekur and its tolerability in female patients suffering from recurrent urinary tract infectioN39.0N30.2Urinary tract infection, site not specifiedOther chronic cystitisDRKS00016760DR. KADE Pharmazeutische Fabrik GmbH81
已完成
不适用
Post-market clinical follow-up (PMCF) study to observe the course of symptoms of vulvovaginal dryness in patients receiving therapy with KadeFungin® BefeuchtungsgelN89.8Other specified noninflammatory disorders of vaginaDRKS00017248DR. KADE Pharmazeutische Fabrik GmbH100
