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Recruiting NCT03607565

A New Parameter Derived From DSA to Evaluate Cerebral Perfusion

Observational Cerebral Ischemia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Cerebral Ischemia. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Association Between a New Parameter Derived From DSA and Outcomes in Cerebral Ischemia

Overview

This observational study focus on a new parameter of cerebral perfusion derived form digital substraction angiography.

Detailed description

Ischemic cerebrovascular disease is an important cause of death and disability in the world. Digital Subtraction Angiography (DSA) is the golden index for evaluating cerebral blood vessels. We introduced a new parameter derived from DSA to evaluate the perfusion to predict the outcomes in acute stroke with large vessel occlusion.

To study the possible relationship between the new parameter of cerebral perfusion derived from DSA and outcomes in cerebral ischemia(modified Rankin Scale), we intend to retrospectively analyze the images derived from patients who undergone the DSA and follow-up outcomes(modified Rankin Scale).

Primary outcome measures

  • the outcomes between good perfusions and poor perfusions [Time frame: 3 months to 2 years]
Secondary outcome measures (1)
  • the outcomes between good perfusions and middle perfusions [Time frame: 3 months to 2 years]

Eligibility criteria

Inclusion criteria

  • Cerebral ischemia
  • patients undergone DSA

Exclusion criteria

1.cerebral hemorrhage

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Xi'an No.3 Hospital — Xi'an

Identifiers

NCT: NCT03607565 · Hnn

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗