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NCT05982015Completed

Efficacy Study II on Remote Ischemic Conditioning for the Prevention of Stroke-Associated Pneumonia

Multicenter, Randomized, Double-blind, Pseudo Treatment-controlled Clinical Study on the Efficacy and Safety of Remote Ischemic Conditioning in Preventing Stroke-associated Pneumonia

Source: ClinicalTrials.gov · Last updated 27 Dec 2024

Brief summary (registry, in English)

Verifying whether remote ischemic adaptation can reduce the occurrence of stroke related pneumonia in acute stroke patients within 24 hours of onset

Status (registry)
Completed
Study type
Interventional
Enrollment
1651 (actual)
First submitted
1 Aug 2023
Start date
22 Jan 2024
Primary completion date
19 Sept 2024
Lead sponsor
Capital Medical University
Diseases
Stroke
NCT number
NCT05982015

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1651
  • From 22 Jan 2024 to the primary completion date, 19 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

  • Anti-infective drug were used within 7 days prior to stroke;
  • Use of immunosuppressive drug within the preceding 3 months;

Other illness

  • Evidence of lung infection, urinary tract infection or other infectious diseases during the screening period
  • Uncontrolled hypertension with medication (defined as systolic blood pressure ≥200 mmHg and/or diastolic blood pressure ≥110 mmHg);
  • There are contraindications for remote ischemic conditioning (such as skin and soft tissue injury, fractures, peripheral arterial disease, etc. in the upper limbs);
  • History of autoimmune disease or malignancies;
  • Other conditions are not suitable for this trial as evaluated by researchers.

Other

  • During the screening period, body temperature ≥ 38 ℃;
  • Expected lifespan less than 7 days
  • Mechanical ventilation is expected to be required within 7 days;
  • Pregnant or lactating, or pregnancy test positive;
  • Current participation in another investigational trial;

Who the study is looking for

  • Age≥18 years old;
  • Diagnosis of acute ischemic stroke;
  • Remote ischemic conditioning or sham-remote ischemic conditioning can be treated within 24 hours after stroke onset
  • NIHSS score≥4;
  • Subject or his or her legally authorized representative was able to provide informed consent.

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
Xuanwu Hospital, Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

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