JPRN-UMIN000042113尚未招募未知
Clinical research on hemodynamic predictors for the progression of major intracranial cerebrovascular stenosis using CFD analysis - CV Stenosis CFD Study
ational Hospital Organization0 个研究点目标入组 650 人开始时间: 2020年10月14日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 650
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
- 20years-old 至 ot applicable(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Cases with stenosis after irradiation 2) Cases with moyamoya disease 3) Cases with stenosis due to dissection 4) Cases with congenital stenosis 5) Cases after bypass surgery on the diseased side (registration is possible if there is an unoperated stenotic lesion on the contralateral side) 6) Patients after angioplasty of the lesion (registration is possible if there are other unoperated stenotic lesions) 7) When the principal investigator and the research coordinator judge that participation in this research is not appropriate
研究者
相似试验
招募中
不适用
Clinical study to evaluate hemodynamic change in exercise test with or without protective maskKCT0005235Chungbuk National University Hospital90
招募中
不适用
Prediction of Hemodynamic Instability in Patients Admitted to the ICU A Prospective, Nonrandomized, Noninterventional Study for Clinical Data CollectioHypotension Probability Indicator (HPI) ICU patients with pressure waveform data. <br />Voorspeller van hemodynamische instabiliteit middels arteriële en non-invasieve drukcurve bij IC patiënten.NL-OMON28259Edwards Lifesciences LLCOne Edwards WayIrvine, CA 92614 USAContact: Jos J SettelsSr Distinguished Engineer, R&D Critical CareEdwards Lifesciences BMEYEHoogoorddreef 60,1101 BE Amsterdam ZuidoostTelephone No.: +31 (0)20 753 3022500
尚未招募
不适用
â??Effects on blood pressure, pulse rate,degree of anaesthesia and analgesia in patients undergoing Caeserian section under lower dose of drug during Spinal Anaesthesiaâ??CTRI/2021/12/038735Ramakrishna Mission Seva Pratisthan And Vivekananda Institute Of Medical Sciences
进行中(未招募)
不适用
Clinical investigation into efficacy, hemodynamics and tolerability of simvastatin vs placebo in patients with pulmonary arterial hypertension(Shorttitle: SIPHT)Double-blind, randomized, prospective Phase III-b study for 6 months with adjusting doses of simvastatin (40/80 mg daily) or placebo followed by an open-label period with a final dose of simvastatin 80 mg daily for another 6 months - SIPHTModified NYHA class II or III patients with Pulmonary Hypertension (PH), ICD: 416.9MedDRA version: 8.1Level: LLTClassification code 10020787Term: Hypertension pulmonaryEUCTR2005-004863-41-DEDept. of Internal Medicine II, University Hospital Giessen40
已完成
不适用
A study comparing general anesthesia and spinal anesthesia in respect to variation in heart rate and blood pressure due to gas insufflation of abdomen in elective laparoscopic appendix operationsCTRI/2018/02/011746Komala B80
