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Clinical Trials/ACTRN12619001274167
ACTRN12619001274167
Recruiting
未知

A pragmatic, multi-centre, patient and assessor-blinded, parallel group, randomised controlled trial (RCT) comparing a ‘standard’ and ‘augmented’ systolic blood pressure strategy during general anaesthesia for endovascular thrombectomy in acute ischaemic stroke

Dr Douglas Campbell0 sites550 target enrollmentSeptember 16, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Stroke
Sponsor
Dr Douglas Campbell
Enrollment
550
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 16, 2019
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr Douglas Campbell

Eligibility Criteria

Inclusion Criteria

  • Adults equal to and greater than 18 years of age who fulfill all of the following inclusion criteria, none of the exclusion criteria, and have undergone an appropriate consenting process.
  • Inclusion criteria
  • Patients diagnosed with anterior circulation stroke (ICA or proximal M1 or M2 segment of MCA) treated with ECR within 6 hrs of stroke onset and ECR patients presenting within 6\-24 hours and favourable penumbra on perfusion scanning (see criteria 1\-3\).
  • Additional criteria in the 6 to 24\-hour window.
  • 1\. ‘wake up’ stroke; CT with no (or at most minimal) acute infarction or
  • 2\. patient 80 years or older (NIHSS of 10 and infarct volume less than 21 ml on DWI or CT perfusion\-CBF)
  • 3\. patient less than 80 years (NIHSS of 10 and infarct volume less than 31 ml on DWI or CT perfusion\-CBF NIHSS of 20 and infarct volume less than 51 ml on DWI or CT perfusion\-CBF).

Exclusion Criteria

  • Rescue”’ procedures eg acute ischaemic stroke associated with major medical procedures such as coronary artery stenting and coronary artery bypass
  • pre\-stroke mRS\>\=3
  • not having GA
  • terminal illness with expected survival \<1 year
  • cardiovascular conditions where BP targeting will be contra\-indicated
  • unable to participate in 3\-month follow up

Outcomes

Primary Outcomes

Not specified

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