NCT04631536
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Managing Endothelial Dysfunction in COVID-19 : A Randomized Controlled Trial at LAUMC |
Active, not recruiting |
Phase 3 |
Jan/10/2021 |
Jul/01/2022 |
- Alternative id - Lebanese American University
- Interventions - Drug: Atorvastatin + L-arginine + Folic acid + Nicorandil + Nebivolol|Drug: Placebo
- Study type - Interventional
- Study results - No Results Available
- Locations - LAUMCRH, Beirut, Lebanon
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double (Participant, Care Provider)|Primary Purpose: Treatment
- Enrollment - 42
- Age - 18 Years and older (Adult, Older Adult)
- Outcome measures - Clinical Improvement|Need for ICU admission or invasive mechanical ventilation|All cause mortality|Occurrence of side effects
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NCT04466241
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Combination Therapies to Reduce Carriage of SARS-Cov-2 and Improve Outcome of COVID-19 in Ivory Coast: a Phase Randomized IIb Trial |
Recruiting |
Phase 2|Phase 3 |
Nov/27/2020 |
Mar/26/2021 |
- Alternative id - ANRS COV01 INTENSE COV
- Interventions - Drug: Lopinavir/Ritonavir 200 MG-50 MG Oral Tablet|Drug: Telmisartan 40Mg Oral Tablet|Drug: Atorvastatin 20 Mg Oral Tablet
- Study type - Interventional
- Study results - No Results Available
- Locations - Service des Maladies Infectieuses et Tropicales, Centre Hospitalier et Universitaire (CHU) Treichville, Abidjan, Côte D'Ivoire|Centre de Traitement des Maladies Infectieuses (CTMI), CHU de Yopougon, Abidjan, Côte D'Ivoire
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
- Enrollment - 294
- Age - 18 Years and older (Adult, Older Adult)
- Outcome measures - Proportion of patients with undetectable nasopharyngeal swab SARS-CoV-2 PCR and C-reactive protein (CRP) < 27 mg/L at Day 11|Proportion of patients with clinical improvement on the 7-point ordinal scale at Day 11 and Day 28|Kinetics of SARS-CoV-2 viral load|Death rate at Day 11 and Day 28|All causes of death and Acute respiratory distress syndrome (ARDS) at Day 28|Time to hospital discharge|Duration of oxygen supplementation|Prevalence of grade III or IV adverse events|Residual concentration of lopinavir, telmisartan and atorvastatin|Evolution of inflammatory and immunological markers (CRP, fibrinogen, ferritin, d-dimer, dosing of IgG, IgA, IgM; TCD4, CD8, B lymphocytes, NK lymphocytes; naïve/memory T lymphocytes)|Evolution of endothelial activation markers (VEGF and soluble VEGF receptor,VE-cadherin, PECAM/CD31, CD42 and angiopoietin-2)|Proportion of patients with good results according to HIV status|Number of contact cases infected by COVID-19 at Day 28
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NCT04904536
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Statin TReatment for COVID-19 to Optimise NeuroloGical recovERy |
Not yet recruiting |
Phase 3 |
Oct/11/2021 |
Jun/01/2023 |
- Alternative id - X21-0113
- Interventions - Drug: Atorvastatin|Other: Standard Care
- Study type - Interventional
- Study results - No Results Available
- Locations - The George Institute for Global Health, Sydney, New South Wales, Australia
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Outcomes Assessor)|Primary Purpose: Treatment
- Enrollment - 400
- Age - 18 Years and older (Adult, Older Adult)
- Outcome measures - Neurological Recovery|Brain Imaging
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NCT04801940
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HElping Alleviate the Longer-term Consequences of COVID-19 (HEAL-COVID) |
Recruiting |
Phase 3 |
May/19/2021 |
Jan/31/2024 |
- Alternative id - A095848
- Interventions - Drug: Apixaban|Drug: Atorvastatin
- Study type - Interventional
- Study results - No Results Available
- Locations - Addenbrookes Hospital, Cambridge, United Kingdom
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
- Enrollment - 2631
- Age - 18 Years and older (Adult, Older Adult)
- Outcome measures - Hospital free survival.|All-cause mortality|Hospital readmission after discharge from index hospital admission|Suspected Serious Adverse Reactions|FACIT-Fatigue|Modified MRC Dyspnoea Scale|COVID-19 core outcome measure for recovery|Patient Health Questionnaire-2 (PHQ-2)|Generalized Anxiety Disorder-2 (GAD-2)|PTSD Checklist (PCL-2)|Quality of life using the EQ5D-5L|Intervention tolerability using the FACT-GP5|Additional disease specific systemic symptoms
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NCT04952350
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Atorvastatin for Reduction of 28-day Mortality in COVID-19: RCT |
Active, not recruiting |
Phase 3 |
Aug/14/2021 |
Apr/01/2022 |
- Alternative id - R.21.04.1300.R1
- Interventions - Drug: Atorvastatin 40 Mg Oral Tablet|Other: Placebo
- Study type - Interventional
- Study results - No Results Available
- Locations - Mansoura University Hospitals, Mansoura, Aldakahlia, Egypt
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment
- Enrollment - 220
- Age - 18 Years and older (Adult, Older Adult)
- Outcome measures - mortality|incidence of invasive mechanical ventilation (IMV)|duration of invasive mechanical ventilation (IMV)|Time to clinical improvement|serious adverse effects|Intensive Care length of stay|acute kidney injury|status at hospital discharge|Hospital length of stay
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NCT04486508
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Intermediate-dose vs Standard Prophylactic Anticoagulation and Statin vs Placebo in ICU Patients With COVID-19 |
Completed |
Phase 3 |
Jul/30/2020 |
Jul/05/2021 |
- Alternative id - 99060
- Interventions - Drug: intermediate dose Enoxaparin/ unfractionated heparin|Drug: standard prophylactic dose Enoxaparin/ unfractionated heparin|Drug: Atorvastatin 20mg|Drug: Matched placebo
- Study type - Interventional
- Study results - No Results Available
- Locations - Masih Daneshvari Hospital, Tehran, Iran, Islamic Republic of
- Study designs - Allocation: Randomized|Intervention Model: Factorial Assignment|Masking: Single (Outcomes Assessor)|Primary Purpose: Treatment
- Enrollment - 600
- Age - 18 Years and older (Adult, Older Adult)
- Outcome measures - a composite of acute VTE, arterial thrombosis, treatment with ECMO, or all-cause mortality|Rate of all-cause mortality|Rate of objectively-confirmed VTE|Ventilator free days|Rate of major bleeding|Rate of clinically-relevant non-major bleeding|Rate of severe thrombocytopenia|Rate of rise in liver enzymes|Clinically-diagnosed myopathy|Objectively-confirmed arterial thrombosis
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NCT04380402
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Atorvastatin as Adjunctive Therapy in COVID-19 |
Recruiting |
Phase 2 |
Jun/25/2020 |
May/08/2022 |
- Alternative id - MountAuburn
- Interventions - Drug: Atorvastatin
- Study type - Interventional
- Study results - No Results Available
- Locations - Mount Auburn Hospital, Cambridge, Massachusetts, United States
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
- Enrollment - 300
- Age - 18 Years to 85 Years (Adult, Older Adult)
- Outcome measures - Proportion of patients that progress to severe or critical requiring ICU admission and/or emergency salvage therapy, or death|Overall score of patients in each arm on Day 7 based on WHO Ordinal Scale for Clinical Improvement|Overall score of patients in each arm on Day 30 based on WHO Ordinal Scale for Clinical Improvement|Proportions of patients in each arm who test negative for SARS-CoV-2 on Day 7
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NCT04333407
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Preventing Cardiac Complication of COVID-19 Disease With Early Acute Coronary Syndrome Therapy: A Randomised Controlled Trial. |
Recruiting |
Not Applicable |
Apr/03/2020 |
Mar/30/2021 |
- Alternative id - 20HH5868
- Interventions - Drug: Aspirin 75mg|Drug: Clopidogrel 75mg|Drug: Rivaroxaban 2.5 MG|Drug: Atorvastatin 40mg|Drug: Omeprazole 20mg
- Study type - Interventional
- Study results - No Results Available
- Locations - Charing Cross Hospital, London, United Kingdom
- Study designs - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
- Enrollment - 3170
- Age - 18 Years to 85 Years (Adult, Older Adult)
- Outcome measures - All-cause mortality at 30 days after admission|Absolute change in serum troponin from admission to peak value|Discharge Rate|Intubation Rate
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NCT04900155
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Evaluation of the Effect of Long-term Lipid-lowering Therapy in STEMI Patients With Coronavirus Infection COVID-19 |
Recruiting |
Not Applicable |
Nov/20/2020 |
May/01/2022 |
- Alternative id - PSU/T-487
- Interventions - Drug: Atorvastatin 80mg|Drug: Atorvastatin-Ezetimibe
- Study type - Interventional
- Study results - No Results Available
- Locations - Valentin Oleynikov, Penza, Russian Federation
- Study designs - Allocation: Non-Randomized|Intervention Model: Sequential Assignment|Masking: None (Open Label)|Primary Purpose: Treatment
- Enrollment - 200
- Age - 30 Years to 70 Years (Adult, Older Adult)
- Outcome measures - Lipid profile assessment|Assessment of ventricular rhythm disturbances|Electrical instability and autonomic regulation of heart rate|Left ventricular systolic function|Left ventricular myocardial deformation (strain, strain rate)|Number of Participants with major cardiovascular events
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