JPRN-jRCT2080221949未知2 期
A Randomized, Double Blind, Multi-center, Placebo-Controlled Exploratory Study of AS-3201 in Patients with Diabetic Sensorimotor Polyneuropathy [Phase II]
适应症
试验速览
- 阶段
- 2 期
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 <= 70age old（—）
- 性别
- All
入选标准
- •Patients with DPN who satisfy the following inclusion criteria
- •-Patients who have DPN symptoms, signs and abnormal nerve conduction on the basis of pre-defined criteria
- •-Outpatients
排除标准
- •-Patients with known non diabetic causes of neuropathic symptoms
- •-Patients with focal or entrapment neuropathy
- •-Patients with a history of epilepsy or serious head injury
研究者
相似试验
进行中（未招募）
不适用
A Double-blind, Randomized, Multi-center, Placebo-controlled, Parallel-group Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in Subjects with Diabetes Mellitus type 2Pancreatic exocrine insufficiency in diabetes type IIEUCTR2013-001347-31-ESAbbott Laboratories GmbH50
已完成
2 期
A phase 2 clincial study to evaluate safety and efficacy of AMG 785 in Skeletally Mature Adults With a Fresh Unilateral Tibial Diaphyseal Fracture Status Post Definitive Fracture Fixation With an Intramedullary NailCTRI/2009/091/001044Amgen Technology Pvt Ltd400
进行中（未招募）
1 期
Efficacy and Safety in a randomised acute pain study of MR308.Acute pain after third molar tooth extractiondental procedure must have involved extraction of at least two impacted third molars requireing bone removal. If only two impacted third molars are extracted, they must be ipsilateral and both required bone removal under local anaesthesia.MedDRA version: 20.1Level: LLTClassification code 10066714Term: Acute painSystem Organ Class: 100000004867EUCTR2016-000592-24-PLMundipharma Research GmbH & Co. KG765
进行中（未招募）
1 期
Efficacy and Safety in a randomised acute pain study of MR308.Acute pain after third molar tooth extractiondental procedure must have involved extraction of at least two impacted third molars requireing bone removal. If only two impacted third molars are extracted, they must be ipsilateral and both required bone removal under local anaesthesia.MedDRA version: 20.0 Level: LLT Classification code 10066714 Term: Acute pain System Organ Class: 100000023314EUCTR2016-000592-24-DEMundipharma Research GmbH & Co. KG726
进行中（未招募）
1 期
Efficacy and Safety in a randomised acute pain study of MR308.Acute pain after open total or subtotal abdominal hysterectomyMedDRA version: 19.0Level: LLTClassification code 10066714Term: Acute painSystem Organ Class: 100000004867EUCTR2016-000593-38-ESMundipharma Research GmbH & Co. KG1,100