Concomitant Use of Clopidogrel With Atorvastatin or Rosuvastatin in Patients With Small Vessel Stroke
NCT06358313 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 600
Last updated 2026-04-23
Summary
Along with the current clinical trial, the impact of adding atorvastatin or rosuvastatin in the first 24 hours on the clinical outcomes of first-ever small vessel stroke patients treated with clopidogrel and aspirin assessed through NIHSS, mRS, and possible adverse effects.
Conditions
Interventions
- DRUG
-
Atorvastatin 40mg
The atorvastatin group consisted of 300 patients who received 40 mg daily atorvastatin for 3 months, and open-label clopidogrel at a loading dose of 300 mg and then 75 mg daily till the end of the 3 months.
- DRUG
-
Rosuvastatin 20mg
The rosuvastatin group consisted of 300 patients who received 40 mg daily rosuvastatin for 3 months, and open-label clopidogrel at a loading dose of 300 mg and then 75 mg daily till the end of the 3 months.
Sponsors & Collaborators
-
Kafrelsheikh University
lead OTHER
Principal Investigators
-
mohamed G. Zeinhom, MD · neurology department kafr el-sheikh university
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-04-10
- Primary Completion
- 2026-05-10
- Completion
- 2026-05-30
- FDA Drug
- Yes
Countries
- Egypt
Study Locations
More Related Trials
-
Comparison of Rosuvastatin and Atorvastatin in Patients With Acute Coronary Syndrome
NCT00665834 ·Status: COMPLETED ·Phase: PHASE4
-
Statins in Patients With Type 2 Diabetes Mellitus and Previous History of Acute Coronary Syndrome
NCT05306990 ·Status: COMPLETED ·Phase: NA
-
Comparison of the Bioavailability of Fenofibric Acid and Rosuvastatin From 5/45 mg Strength of ABT-143 Relative to That From the Coadministration of ABT-335 (Fenofibric Acid) 45 mg and Rosuvastatin Calcium 5 mg
NCT00826358 ·Status: COMPLETED ·Phase: PHASE1
-
Prospective Evaluation of Proteinuria and Renal Function in Non-diabetic Patients With Progressive Renal Disease
NCT00296400 ·Status: COMPLETED ·Phase: PHASE2
-
Registry On Efficacy and Safety Of Rosuvastatin, and Atorvastatin and Simvastatin In Hypercholesterolaemia
NCT01352897 ·Status: COMPLETED
-
Study on Rosuvastatin+Ezetimibe and Rosuvastatin for LDL-C Goal in Patients With Recent Ischemic Stroke
NCT03993236 ·Status: COMPLETED ·Phase: PHASE4
-
Comparison of the Bioavailability of Fenofibric Acid and Rosuvastatin From ABT-143 Relative to That From the Coadministration of ABT-335 (Fenofibric Acid) and Rosuvastatin Calcium
NCT00808678 ·Status: COMPLETED ·Phase: PHASE1
-
Prospective Evaluation of Proteinuria and Renal Function in Diabetic Patients With Progressive Renal Disease
NCT00296374 ·Status: COMPLETED ·Phase: PHASE2
-
A Study To Evaluate the Effect of Rosuvastatin On Intravascular Ultrasound-Derived Coronary Atheroma Burden (ASTEROID)
NCT00240318 ·Status: COMPLETED ·Phase: PHASE3
-
Interaction Between ABT-335, Rosuvastatin and Warfarin
NCT00487136 ·Status: COMPLETED ·Phase: PHASE1
-
Switching to Rosuvastatin Versus Adding Ezetimibe to Atorvastatin Versus Doubling the Dose of Atorvastatin in Patients With Hypercholesterolemia and Risk Factors (P03708)
NCT00651378 ·Status: TERMINATED ·Phase: PHASE4
-
Pharmacodynamic Comparison of Rosuvastatin Versus Atorvastatin on Platelet Reactivity in Patients With Coronary Artery Disease on Dual Antiplatelet Therapy With New P2Y12 Inhibitors (Trial gRANADa)
NCT02030054 ·Status: UNKNOWN ·Phase: PHASE4
-
Drug-Drug Interaction Study to Assess the Effects of Steady State Pitavastatin 4 mg or Rosuvastatin 40 mg on Steady-State Warfarin in Healthy Adult Volunteers
NCT01178853 ·Status: COMPLETED ·Phase: PHASE4
-
A Comparative Study of Rosuvastatin and Atorvastatin in Patients With Hyperlipidemia
NCT02979704 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
To Estimate the Potential Effects of Repeat Doses of Darapladib on the Pharmacokinetics (PK) of Rosuvastatin as Well as Evaluating Safety and Tolerability in Healthy Volunteers
NCT01751074 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluation of the Efficacy of Rosuvastatin in Daily Practice in Untreated High Risk Patients (CHALLENGE)
NCT00574782 ·Status: COMPLETED
-
30 Week Study of the Combination of ABT-335 and Rosuvastatin Compared to Rosuvastatin Monotherapy for Subjects With Dyslipidemia and Stage 3 Chronic Kidney Disease
NCT00680017 ·Status: COMPLETED ·Phase: PHASE3
-
Investigation of Interactions Between Faldaprevir, Itraconazole, Atorvastatin and Rosuvastatin
NCT01795937 ·Status: COMPLETED ·Phase: PHASE1
-
Compare the Efficacy of Rosuvastatin to Atorvastatin in High Risk Patients With Hypercholesterolemia
NCT00683618 ·Status: COMPLETED ·Phase: PHASE3
-
STELLAR-Rosuvastatin vs. Atorvastatin, Pravastatin, Simvastatin Across Dose Ranges
NCT00654537 ·Status: COMPLETED ·Phase: PHASE3
-
Type III Dysbetalipoproteinemia
NCT00214604 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of Rosuvastatin in Intracerebral Hemorrhage
NCT00364559 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess the Effect of AZD0780 on the Pharmacokinetics of Rosuvastatin.
NCT05787002 ·Status: COMPLETED ·Phase: PHASE1
-
COMETS - Compare the Efficacy of Rosuvastatin With Atorvastatin and Placebo in the Treatment of Non-Diabetic, Non-Atheroscleric, Metabolic Syndrome Subjects
NCT00654485 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Investigate the Interaction of GSK1292263 With Rosuvastatin and Simvastatin in Healthy Subjects
NCT01101568 ·Status: COMPLETED ·Phase: PHASE1