Skip to main content
Clinical Trials/JPRN-UMIN000042113
JPRN-UMIN000042113
Not yet recruiting
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 sites650 target enrollmentOctober 14, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
major intracranial artery stenosis
Sponsor
ational Hospital Organization
Enrollment
650
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 14, 2020
End Date
March 31, 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
ational Hospital Organization

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

Similar Trials

Recruiting
Not Applicable
Clinical study to evaluate hemodynamic change in exercise test with or without protective mask
KCT0005235Chungbuk National University Hospital90
Recruiting
Not Applicable
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
Not yet recruiting
Not Applicable
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??Health Condition 1: O82- Encounter for cesarean delivery without indicationHealth Condition 2: O- Medical and Surgical
CTRI/2021/12/038735Ramakrishna Mission Seva Pratisthan And Vivekananda Institute Of Medical Sciences
Active, not recruiting
Not Applicable
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 pulmonary
EUCTR2005-004863-41-DEDept. of Internal Medicine II, University Hospital Giessen40
Completed
Not Applicable
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 operationsHealth Condition 1: null- ASA 1 and ASA 2Health Condition 2: K358- Other and unspecified acute appendicitis
CTRI/2018/02/011746Komala B80