Acetylsalicylic Acid in the Prevention of Severe SARS-CoV2 Pneumonia in Hospitalised Patients With COVID-19 (Asperum)
Multicenter Randomized, Double-blind, Placebo-controlled, Clinical Trial of Acetylsalicylic Acid in the Prevention of Severe SARS-CoV2 Pneumonia in Hospitalised Patients (Asperum)
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Phase
Phase
- Phase 3
Contacts and Locations
Study Contact
Study Contact
- Name: Pietro Minuz, Professor
- Phone Number: +39 045-8124414
- Email: pietro.minuz@univr.it
Study Contact Backup
- Name: Marco Cattaneo, Professor
- Phone Number: +390250323095
- Email: marco.cattaneo@unimi.it
Study Locations
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-
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Verona, Italy, 37126
- Azienda Ospedaliera Universitaria Integrata Verona
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- in a medical area ward dedicated to Covid-19 patients
- Positivity by RT_PCR of the search for genetic material of SARS-CoV2
- Covid-19 pneumonia with moderate clinical picture based on clinical parameters
- O2 saturation> 94% with maximum FiO2 32%
- Respiratory acts <30 / minute
- age >18 years
- Consent to participate in the study
Exclusion Criteria:
- Any Antithrombotic treatment including acetylsalicylic acid
- Active Bacterial infection
- Active or in maintenance therapy neoplasm
- Inability to provide consent
- Any contraindication to the acetylsalicylic acid use
- Active peptic disease
- Active Major pathological bleeding
- Recent (<30 days) major bleeding
- Recent intracranial bleeding
- Need to use therapeutic doses of oral anticoagulants or heparins
- Need to use combination antiplatelet drugs for clinical indication
- Hypersensitivity to acetylsalicylic acid or to any of the excipients
- Hypersensitivity to non-steroidal anti-inflammatory drugs (NSAIDs)
- Severe hepatic insufficiency (Child-Pugh class C).
- Severe heart failure (NYHA class 3-4)
- Platelet count less than 150000 / mmc
- Haemostasis alteration (INR> 1.5, APTT> 1.5)
- Plasma fibrinogen <100 mg / dL
- Blood pressure >160/100 mmHg
- Concomitant treatment with serotonin reuptake inhibitors
- Participation in another pharmacological clinical trial
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Active Comparator: Acetylsalicylic acid
Tablets of 100 mg acetylsalicylic acid (one 100 mg daily dose.
On the first day a loading dose of 300 mg will be administered)
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administration of one tablet daily for 15 days.
On the first day a loading dose of 300 mg will be administered
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Placebo Comparator: Placebo
Tablets of placebo, identical to active comparator (one tablet daily dose.
On the first day 3 tablets will be administered)
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administration of one tablet daily for 15 days.
On the first day 3 tablets will be administered
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevention of clinical worsening
Time Frame: day 15
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Transfer to ICU
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day 15
|
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Prevention of lung function worsening
Time Frame: day 15
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PaO2/FiO2 lower than 150 mm Hg
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day 15
|
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Prevention of death
Time Frame: day 15
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Death for any cause
|
day 15
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in body temperature
Time Frame: Daily for 15 days
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Body temperature
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Daily for 15 days
|
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Change in oxygen saturation
Time Frame: Daily for 15 days
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Oxygen saturation
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Daily for 15 days
|
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Change in blood gases
Time Frame: Daily for 15 days
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blood gas analysis
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Daily for 15 days
|
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Change in blood cell count
Time Frame: Daily for 15 days
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blood cell count
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Daily for 15 days
|
|
Change in blood oxygen
Time Frame: Daily for 15 days
|
Oxygen administration when O2 saturation <92%
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Daily for 15 days
|
|
Change in clinical markers of lung function
Time Frame: Daily for 15 days
|
PaO2/FiO2; progression of disease at Rx
|
Daily for 15 days
|
|
Change in clinical markers of liver damage
Time Frame: Daily for 15 days
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markers of organ damage (ALT)
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Daily for 15 days
|
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Change in clinical markers of hearth damage
Time Frame: Daily for 15 days
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markers of organ damage (troponin)
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Daily for 15 days
|
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Change in clinical markers of renal damage
Time Frame: Daily for 15 days
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markers of organ damage (creatinine)
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Daily for 15 days
|
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Effects on blood cell count
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers (blood cell count)
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Baseline, day 1, 2, 7 and 15.
|
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Effects on CRP
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers (CRP)
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Baseline, day 1, 2, 7 and 15.
|
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Effects on D-dimer
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers (D-dimer)
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Baseline, day 1, 2, 7 and 15.
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Effects on interleukin-1
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers ( IL-1)
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Baseline, day 1, 2, 7 and 15.
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Effects on interleukin-6
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers (IL-6)
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Baseline, day 1, 2, 7 and 15.
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Effects on fibrinogen
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers (fibrinogen)
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Baseline, day 1, 2, 7 and 15.
|
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Effects on plasma albumin
Time Frame: Baseline, day 1, 2, 7 and 15.
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Inflammatory markers (albumin)
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Baseline, day 1, 2, 7 and 15.
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Effects on protrombin time
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (prothrombin time)
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Baseline, day 1, 2, 7 and 15.
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Effects on activated partial thromboplastin time
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (activated partial thromboplastin time)
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Baseline, day 1, 2, 7 and 15.
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Effects on serum thromboxane
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets ( serum TxB2)
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Baseline, day 1, 2, 7 and 15.
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Effects on thromboxane metabolite
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (urinary 11-dehydro TXB2)
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Baseline, day 1, 2, 7 and 15.
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Effects on platelet count
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (platelet count)
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Baseline, day 1, 2, 7 and 15.
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Effects on reticulated platelets
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (reticulated platelets)
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Baseline, day 1, 2, 7 and 15.
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Effects on platelet/leukocyte conjugates
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (platelets/leukocytes conjugates)
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Baseline, day 1, 2, 7 and 15.
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Effects on plasma P-selectin
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (plasma P-selectin)
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Baseline, day 1, 2, 7 and 15.
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Effects on P-selectin expression
Time Frame: Baseline, day 1, 2, 7 and 15.
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platelet and hemostatic markets (platelet expression of P-selectin)
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Baseline, day 1, 2, 7 and 15.
|
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Clincal mixed outcome of lung function, ROX score
Time Frame: Days 7 and 15
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ROX score
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Days 7 and 15
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Clincal mixed outcome of lung function, SOfa score
Time Frame: Days 7 and 15
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SOfa score
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, Apache index
Time Frame: Days 7 and 15
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Apache index
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, need to perform CT scan due to worsening of blood gases
Time Frame: Days 7 and 15
|
need to perform CT scan due to worsening of blood gases
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, need to transfer the patient to ICU
Time Frame: Days 7 and 15
|
need to transfer the patient to ICU
|
Days 7 and 15
|
|
Clincal mixed outcome of lung function, need for mechanical ventilation
Time Frame: Days 7 and 15
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need for mechanical ventilation
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, days without need of mechanical ventilation
Time Frame: Days 7 and 15
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days without need of mechanical ventilation
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, venous thromboembolism
Time Frame: Days 7 and 15
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venous thromboembolism
|
Days 7 and 15
|
|
Clincal mixed outcome of lung function, pulmonary thrombosis
Time Frame: Days 7 and 15
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pulmonary thrombosis
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, cardiovascular event
Time Frame: Days 7 and 15
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cardiovascular event
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, death
Time Frame: Days 7 and 15
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death
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, multiorgan failure
Time Frame: Days 7 and 15
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multiorgan failure
|
Days 7 and 15
|
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Clincal mixed outcome of lung function, discharge due to resolution of signs and symptoms
Time Frame: Days 7 and 15
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discharge due to resolution of signs and symptoms
|
Days 7 and 15
|
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Safety outcomes, Major or clinically relevant bleeding
Time Frame: days 1,2,7 and 15
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Major or clinically relevant bleeding
|
days 1,2,7 and 15
|
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Safety outcomes, total bleeding based on ISTH bleeding score
Time Frame: days 1,2,7 and 15
|
total bleeding based on ISTH bleeding score
|
days 1,2,7 and 15
|
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Safety outcomes, minor bleeding according to ISTH BS
Time Frame: days 1,2,7 and 15
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minor bleeding according to ISTH BS
|
days 1,2,7 and 15
|
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Safety outcomes, decrease in platelet count below 100x109/L
Time Frame: days 1,2,7 and 15
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decrease in platelet count below 100x109/L
|
days 1,2,7 and 15
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Safety outcomes, decrease of al least 2 g/dl Hb levels
Time Frame: days 1,2,7 and 15
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decrease of al least 2 g/dl Hb levels
|
days 1,2,7 and 15
|
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Safety outcomes, need for blood transfusion
Time Frame: days 1,2,7 and 15
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need for blood transfusion
|
days 1,2,7 and 15
|
|
Safety outcomes, alterations of clinical or laboratory parameters
Time Frame: days 1,2,7 and 15
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alterations of clinical or laboratory parameters
|
days 1,2,7 and 15
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Director: Pietro Minuz, Professor, University of Verona, AOUI Verona
- Study Director: Marco Cattaneo, Professor, University of Milan
- Study Director: Roberto Leone, Professor, Universita di Verona
Publications and helpful links
General Publications
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- Tang N, Li D, Wang X, Sun Z. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020 Apr;18(4):844-847. doi: 10.1111/jth.14768. Epub 2020 Mar 13.
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- Chen G, Wu D, Guo W, Cao Y, Huang D, Wang H, Wang T, Zhang X, Chen H, Yu H, Zhang X, Zhang M, Wu S, Song J, Chen T, Han M, Li S, Luo X, Zhao J, Ning Q. Clinical and immunological features of severe and moderate coronavirus disease 2019. J Clin Invest. 2020 May 1;130(5):2620-2629. doi: 10.1172/JCI137244.
- Jackson SP, Darbousset R, Schoenwaelder SM. Thromboinflammation: challenges of therapeutically targeting coagulation and other host defense mechanisms. Blood. 2019 Feb 28;133(9):906-918. doi: 10.1182/blood-2018-11-882993. Epub 2019 Jan 14.
- Varga Z, Flammer AJ, Steiger P, Haberecker M, Andermatt R, Zinkernagel AS, Mehra MR, Schuepbach RA, Ruschitzka F, Moch H. Endothelial cell infection and endotheliitis in COVID-19. Lancet. 2020 May 2;395(10234):1417-1418. doi: 10.1016/S0140-6736(20)30937-5. Epub 2020 Apr 21. No abstract available.
- Margraf A, Zarbock A. Platelets in Inflammation and Resolution. J Immunol. 2019 Nov 1;203(9):2357-2367. doi: 10.4049/jimmunol.1900899.
- Becattini C, Agnelli G, Schenone A, Eichinger S, Bucherini E, Silingardi M, Bianchi M, Moia M, Ageno W, Vandelli MR, Grandone E, Prandoni P; WARFASA Investigators. Aspirin for preventing the recurrence of venous thromboembolism. N Engl J Med. 2012 May 24;366(21):1959-67. doi: 10.1056/NEJMoa1114238. Erratum In: N Engl J Med. 2012 Oct 18;367(16):1573.
- Simes J, Becattini C, Agnelli G, Eikelboom JW, Kirby AC, Mister R, Prandoni P, Brighton TA; INSPIRE Study Investigators (International Collaboration of Aspirin Trials for Recurrent Venous Thromboembolism). Aspirin for the prevention of recurrent venous thromboembolism: the INSPIRE collaboration. Circulation. 2014 Sep 23;130(13):1062-71. doi: 10.1161/CIRCULATIONAHA.114.008828. Epub 2014 Aug 25.
- Sexton TR, Zhang G, Macaulay TE, Callahan LA, Charnigo R, Vsevolozhskaya OA, Li Z, Smyth S. Ticagrelor Reduces Thromboinflammatory Markers in Patients With Pneumonia. JACC Basic Transl Sci. 2018 Aug 28;3(4):435-449. doi: 10.1016/j.jacbts.2018.05.005. eCollection 2018 Aug.
- Yin S, Huang M, Li D, Tang N. Difference of coagulation features between severe pneumonia induced by SARS-CoV2 and non-SARS-CoV2. J Thromb Thrombolysis. 2021 May;51(4):1107-1110. doi: 10.1007/s11239-020-02105-8.
- Minuz P, Mansueto G, Mazzaferri F, Fava C, Dalbeni A, Ambrosetti MC, Sibani M, Tacconelli E. High rate of pulmonary thromboembolism in patients with SARS-CoV-2 pneumonia. Clin Microbiol Infect. 2020 Nov;26(11):1572-1573. doi: 10.1016/j.cmi.2020.06.011. Epub 2020 Jun 18. No abstract available.
- Cattaneo M, Bertinato EM, Birocchi S, Brizio C, Malavolta D, Manzoni M, Muscarella G, Orlandi M. Pulmonary Embolism or Pulmonary Thrombosis in COVID-19? Is the Recommendation to Use High-Dose Heparin for Thromboprophylaxis Justified? Thromb Haemost. 2020 Aug;120(8):1230-1232. doi: 10.1055/s-0040-1712097. Epub 2020 Apr 29. No abstract available.
- Bianconi V, Violi F, Fallarino F, Pignatelli P, Sahebkar A, Pirro M. Is Acetylsalicylic Acid a Safe and Potentially Useful Choice for Adult Patients with COVID-19 ? Drugs. 2020 Sep;80(14):1383-1396. doi: 10.1007/s40265-020-01365-1.
- Carestia A, Davis RP, Grosjean H, Lau MW, Jenne CN. Acetylsalicylic acid inhibits intravascular coagulation during Staphylococcus aureus-induced sepsis in mice. Blood. 2020 Apr 9;135(15):1281-1286. doi: 10.1182/blood.2019002783.
- Chow JH, Khanna AK, Kethireddy S, Yamane D, Levine A, Jackson AM, McCurdy MT, Tabatabai A, Kumar G, Park P, Benjenk I, Menaker J, Ahmed N, Glidewell E, Presutto E, Cain S, Haridasa N, Field W, Fowler JG, Trinh D, Johnson KN, Kaur A, Lee A, Sebastian K, Ulrich A, Pena S, Carpenter R, Sudhakar S, Uppal P, Fedeles BT, Sachs A, Dahbour L, Teeter W, Tanaka K, Galvagno SM, Herr DL, Scalea TM, Mazzeffi MA. Aspirin Use Is Associated With Decreased Mechanical Ventilation, Intensive Care Unit Admission, and In-Hospital Mortality in Hospitalized Patients With Coronavirus Disease 2019. Anesth Analg. 2021 Apr 1;132(4):930-941. doi: 10.1213/ANE.0000000000005292.
- Connors JM, Levy JH. COVID-19 and its implications for thrombosis and anticoagulation. Blood. 2020 Jun 4;135(23):2033-2040. doi: 10.1182/blood.2020006000.
- Gu SX, Tyagi T, Jain K, Gu VW, Lee SH, Hwa JM, Kwan JM, Krause DS, Lee AI, Halene S, Martin KA, Chun HJ, Hwa J. Thrombocytopathy and endotheliopathy: crucial contributors to COVID-19 thromboinflammation. Nat Rev Cardiol. 2021 Mar;18(3):194-209. doi: 10.1038/s41569-020-00469-1. Epub 2020 Nov 19.
- Hottz ED, Azevedo-Quintanilha IG, Palhinha L, Teixeira L, Barreto EA, Pao CRR, Righy C, Franco S, Souza TML, Kurtz P, Bozza FA, Bozza PT. Platelet activation and platelet-monocyte aggregate formation trigger tissue factor expression in patients with severe COVID-19. Blood. 2020 Sep 10;136(11):1330-1341. doi: 10.1182/blood.2020007252.
- Koupenova M, Corkrey HA, Vitseva O, Manni G, Pang CJ, Clancy L, Yao C, Rade J, Levy D, Wang JP, Finberg RW, Kurt-Jones EA, Freedman JE. The role of platelets in mediating a response to human influenza infection. Nat Commun. 2019 Apr 16;10(1):1780. doi: 10.1038/s41467-019-09607-x.
- Marongiu F, Mameli A, Grandone E, Barcellona D. Pulmonary Thrombosis: A Clinical Pathological Entity Distinct from Pulmonary Embolism? Semin Thromb Hemost. 2019 Nov;45(8):778-783. doi: 10.1055/s-0039-1696942. Epub 2019 Sep 19.
- Middleton EA, He XY, Denorme F, Campbell RA, Ng D, Salvatore SP, Mostyka M, Baxter-Stoltzfus A, Borczuk AC, Loda M, Cody MJ, Manne BK, Portier I, Harris ES, Petrey AC, Beswick EJ, Caulin AF, Iovino A, Abegglen LM, Weyrich AS, Rondina MT, Egeblad M, Schiffman JD, Yost CC. Neutrophil extracellular traps contribute to immunothrombosis in COVID-19 acute respiratory distress syndrome. Blood. 2020 Sep 3;136(10):1169-1179. doi: 10.1182/blood.2020007008.
- Patrono C, Baigent C. Role of aspirin in primary prevention of cardiovascular disease. Nat Rev Cardiol. 2019 Nov;16(11):675-686. doi: 10.1038/s41569-019-0225-y. Epub 2019 Jun 26.
- Pulavendran S, Rudd JM, Maram P, Thomas PG, Akhilesh R, Malayer JR, Chow VTK, Teluguakula N. Combination Therapy Targeting Platelet Activation and Virus Replication Protects Mice against Lethal Influenza Pneumonia. Am J Respir Cell Mol Biol. 2019 Dec;61(6):689-701. doi: 10.1165/rcmb.2018-0196OC.
- Scavone M, Rizzo J, Femia EA, Podda GM, Bossi E, Caberlon S, Paroni R, Cattaneo M. Patients with Essential Thrombocythemia may be Poor Responders to Enteric-Coated Aspirin, but not to Plain Aspirin. Thromb Haemost. 2020 Oct;120(10):1442-1453. doi: 10.1055/s-0040-1714351. Epub 2020 Jul 27.
- Taus F, Salvagno G, Cane S, Fava C, Mazzaferri F, Carrara E, Petrova V, Barouni RM, Dima F, Dalbeni A, Romano S, Poli G, Benati M, De Nitto S, Mansueto G, Iezzi M, Tacconelli E, Lippi G, Bronte V, Minuz P. Platelets Promote Thromboinflammation in SARS-CoV-2 Pneumonia. Arterioscler Thromb Vasc Biol. 2020 Dec;40(12):2975-2989. doi: 10.1161/ATVBAHA.120.315175. Epub 2020 Oct 14.
Study record dates
Study Major Dates
Study Start (Anticipated)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Pneumonia, Viral
- Lung Diseases
- Embolism and Thrombosis
- COVID-19
- Pneumonia
- Thrombosis
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Peripheral Nervous System Agents
- Enzyme Inhibitors
- Analgesics
- Sensory System Agents
- Anti-Inflammatory Agents, Non-Steroidal
- Analgesics, Non-Narcotic
- Anti-Inflammatory Agents
- Antirheumatic Agents
- Fibrinolytic Agents
- Fibrin Modulating Agents
- Platelet Aggregation Inhibitors
- Cyclooxygenase Inhibitors
- Antipyretics
- Aspirin
Other Study ID Numbers
Other Study ID Numbers
- EudraCT 2020-006130-12
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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