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NCT04977869Completed

Safety and Efficacy Study of Remote Ischemic Conditioning Combined With Endovascular Thrombectomy for Acute Ischemic Stroke Due to Large Vessel Occlusion of Anterior Circulation

Safety and Efficacy Study of Remote Ischemic Conditioning Combined With Endovascular Thrombectomy for Acute Ischemic Stroke Due to Large Vessel Occlusion of Anterior Circulation: A Multicenter, Randomized, Parallel-controlled Clinical Trial

Source: ClinicalTrials.gov · Last updated 16 Dec 2024

Brief summary (registry, in English)

The purpose of this study is to determine the efficacy and safety of remote ischemic conditioning for patients of acute ischemic stroke who underwent endovascular thrombectomy due to large vessel occlusion of anterior circulation.

Status (registry)
Completed
Study type
Interventional
Enrollment
498 (actual)
First submitted
13 Jul 2021
Start date
26 Aug 2021
Primary completion date
16 Sept 2024
Lead sponsor
Yi Yang
Diseases
Stroke
NCT number
NCT04977869

What you commit to

  • Study type: Interventional
  • Participants enrolled: 498
  • From 26 Aug 2021 to the primary completion date, 16 Sept 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.

Prior treatment

  • 5\) Previous remote ischemic conditioning therapy or similar treatment
  • 9\) Current or past participation in other clinical research, or participation in this study within 3 months prior to admission

Other illness

  • 2\) Contraindication of remote ischemic conditioning, such as severe soft tissue injury, fracture, or vascular injury in the upper limb, acute or subacute venous thrombosis, arterial occlusive disease, and subclavian steal syndrome
  • 10\) Other conditions that the researchers think make the patient unsuitable for the study

Other

  • 1\) Contraindication of endovascular thrombectomy
  • 3\) Head CT showing cerebral hernia and midline displacement
  • 4\) Pregnancy or lactation
  • 6\) Severe hepatic and renal dysfunction
  • 7\) Life expectancy of less than 3 months or inability to complete the study for other reasons
  • 8\) Unwilling to be followed up or poor compliance

Who the study is looking for

  • 1\) Age ≥ 18 years, male or female
  • 2\) Diagnosis of acute ischemic stroke within 24 hours of symptom onset and underwent endovascular thrombectomy (EVT) adhering to current guidelines for large vessel occlusion in the anterior circulation (confirmed by computed tomography angiography or digital subtraction angiography)
  • 3\) Pre-EVT NIHSS ≥ 6
  • 4\) Premorbid mRS ≤ 2
  • 5\) Written informed consent obtained from the patient or legally responsible person

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. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Hospital of Jilin University
Coordinator of this site? Confirm its status
ChangchunChinaUnknown status

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