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NCT06242145CompletedPhase 3

Clopidogrel Versus Cilostazol in Large-vessel Ischemic Stroke

Clopidogrel Versus Cilostazol in Large-vessel Ischemic Stroke, a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 20 Aug 2024

Brief summary (registry, in English)

Along with the current clinical trial, the efficacy and safety of a 300 mg loading dose of ticagrelor administered within 24 hours of the first-ever large-vessel ischemic stroke compared to 200 mg cilostazol were assessed through NIHSS, mRS, and possible adverse effects.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
580 (actual)
First submitted
27 Jan 2024
Start date
1 Jan 2023
Primary completion date
1 Jul 2024
Lead sponsor
Kafrelsheikh University
Diseases
Stroke
NCT number
NCT06242145

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 580
  • From 1 Jan 2023 to the primary completion date, 1 Jul 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

  • The investigators excluded patients who had clinical seizures at the onset of their stroke, as well as those who had symptoms of any major organ failure, active malignancies, or an acute myocardial infarction within the previous six weeks, and those who were on warfarin, regular ticagrelor during the week before admission, or chemotherapy within the previous year.
  • Patients with contraindications to the study drugs were excluded.

Other illness

  • \- The investigators excluded patients who had not been followed up on for 90 days after enrollment, those with NIHSS ≤ 3 or ≥ 25 or who had rapidly resolving symptoms before imaging results, and patients with a known history of persistent or recurrent CNS pathology (e.g., epilepsy, meningioma, multiple sclerosis, history of head trauma with a residual neurological deficit).
  • The investigators excluded patients with active peptic ulcers, GIT surgery, bleeding history within the last year, and those with a history of major surgery within the last three months.
  • The investigators excluded pregnant and lactating patients and those with stroke due to venous thrombosis and stroke following cardiac arrest or profuse hypotension ineligible for our trial.

Lab values

  • The investigators ruled out of our trial patients who had a known allergy to the study drugs and those with INR \> 1.4 or P.T. \>18 or blood glucose level \< 50 or \> 400 mg/DL or blood pressure \< 90/60 or \> 185/110 mmHg on admission or Platelets \< 100,000.

Who the study is looking for

  • the investigators included both genders with eligible ages ranging between 18-75 years, with the first-ever presentation with acute large-vessel ischemic stroke who received antiplatelet treatment within the first 24 hours of the onset of ischemic stroke. Patients with previous transient ischemic attacks (TIA) were not excluded from the study. Patients are not eligible for rt-PA treatment

Age in the registry: 18 years to 75 years · 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
Kafr-Elsheikh University Hospital
Coordinator of this site? Confirm its status
Kafr ash ShaykhEgyptUnknown status

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