A New Parameter Derived From DSA to Evaluate Cerebral Perfusion
ConditionCerebral Ischemia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorXi'an No.3 Hospital
About this trial
This observational study focus on a new parameter of cerebral perfusion derived form digital substraction angiography.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Cerebral ischemia
patients undergone DSA
Disqualifiers
None
Trial population
the study population is from primary care clinic
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Not listed
Trial groups
30,000 Participants
are grouped into 3 trial groupsGroup A: good perfusion in DSA
Group B: middle perfusion in DSA
Group C: poor perfusion in DSA
Trial outcomes
Primary outcomes
1
the outcomes between good perfusions and poor perfusions
Results are reported as odds ratios (ORs) with 95% confidence intervals (CIs).
Time frame
3 months to 2 yearsSecondary outcomes
1
the outcomes between good perfusions and middle perfusions
Results are reported as odds ratios (ORs) with 95% confidence intervals (CIs).
Time frame
3 months to 2 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov