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NCT05517109Completed

Hemodynamic in Postreperfusion Period and Functional Recovery in Acute Ischemic Stroke Patients

The Influence of Different Hemodynamic Parameters in First 24 Hours After Intravenous Thrombolysis on Acute Ischemic Stroke Outcomes: a Randomised Clinical Trial

Source: ClinicalTrials.gov · Last updated 30 Oct 2024

Brief summary (registry, in English)

The investigators are suggtesting that lower goals of systolic blood pressure after intravenous thrombolysis may reduce the risk of hemorrhagic complications and improve functional outcomes after acute ischemic stroke.

Status (registry)
Completed
Study type
Interventional
Enrollment
90 (actual)
First submitted
6 Aug 2022
Start date
12 Mar 2022
Primary completion date
30 Apr 2024
Lead sponsor
Northern State Medical University
Diseases
Stroke
NCT number
NCT05517109

What you commit to

  • Study type: Interventional
  • Participants enrolled: 90
  • From 12 Mar 2022 to the primary completion date, 30 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • failure to achieve hemodynamic goal for 20 minutes before the start of intravenous thrombolysis
  • failure to achieve hemodynamic goal for 60 minutes in first 24 hours after intravenous thrombolysis
  • unfavorable effect development (e.g. seizures, angioedema)

Other

  • absence of informed consent or council of physician agreement
  • pregnancy
  • patients participainting in other clinical trial in the last 90 days
  • any absolute contraindications to intravenous thrombolysis
    • Сompletion criteria:
  • relative arterial hypotension (SBP \<100 mmHg for 60 minutes in first 24 hours after intravenous thrombolysis)
  • informed consent is retracted

Criteria the registry did not label

  • Inclusion сriteria:
  • ischemic stroke diagnosis
  • performed intravenous thrombolysis (including "wake up stroke")
  • systolic blood pressure \>140 mmHg
  • informed consent or council of physician agreement

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
City Hospital # 1 n.a. E.E. Volosevich
Coordinator of this site? Confirm its status
ArkhangelskRussiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.