COVID-19 Clinical Trial
— CAPTOCOVIDOfficial title:
Efficacy of Captopril Nebulization in Covid-19 Patients Suffering of SARS CoV-2 Pneumonia. A Randomized Phase II Study
Captopril being an effective drug available in liquid preparation, administration by nebulization could be of interest for maximizing lung action and minimizing systemic side effects. Such a treatment might be used for "Covid-19" patients with pneumonia in order to avoid ARDS.
Status | Not yet recruiting |
Enrollment | 230 |
Est. completion date | August 2020 |
Est. primary completion date | July 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Hospitalization for acute respiratory failure requiring oxygen administration =3L/mn 2. Age > 18 years or older 3. Presence of pneumonia 4. PCR SARS-CoV-2 positive in any biological sample in the last 7 days 5. Patient affiliated to social security regime 6. Written informed consent provided by the patient or alternatively by next-of-kin, or in emergency situations, prior to any protocol-specific procedures Exclusion Criteria: 1. Decision of withholding invasive mechanical ventilation 2. Shock requiring vasopressor infusion 3. Co-infection with another respiratory pathogen which could be responsible of pneumonia 4. Hypersensitivity to captopril, to any other angiotensin converting enzyme inhibitor or any of the excipients of the specialty used 5. History of angio-oedema 6. History of ACE-inhibitor allergy 7. Known pregnancy or current lactation: Female subject of childbearing potential should have a negative serum pregnancy test prior to receiving the first dose of study medication. 8. Patient who is currently enrolled in other investigational study; 9. Persons deprived of their liberty by judicial or administrative decision, 10. Persons under legal protection/safeguard of justice, 11. Patients under duress psychiatric care, 12. Persons admitted to a health or social institution 13. Patient on state medical aid |
Country | Name | City | State |
---|---|---|---|
France | CH Victor Dupuy- Argenteuil | Argenteuil | |
France | Hôpital Avicenne | Bobigny | |
France | Hôpital Avicenne | Bobigny | |
France | Hôpital Avicenne, | Bobigny | |
France | Hôpital Antoine Béclère | Clamart | |
France | CH de Compiègne-Noyon | Compiègne | |
France | Groupe hospitalier Sud Ile de France | Melun | |
France | Hôpital de la Pitié- Salpêtrière | Paris | |
France | Hôpital Tenon | Paris | |
France | CHRU de Tours, Hôpital Bretonneau | Tours | |
France | Hôpital de Tours | Tours |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique - Hôpitaux de Paris |
France,
Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, Liu L, Shan H, Lei CL, Hui DSC, Du B, Li LJ, Zeng G, Yuen KY, Chen RC, Tang CL, Wang T, Chen PY, Xiang J, Li SY, Wang JL, Liang ZJ, Peng YX, Wei L, Liu Y, Hu YH, Peng P, Wang JM, Liu JY, Chen Z, Li G, Zheng ZJ — View Citation
Gurwitz D. Angiotensin receptor blockers as tentative SARS-CoV-2 therapeutics. Drug Dev Res. 2020 Mar 4. doi: 10.1002/ddr.21656. [Epub ahead of print] — View Citation
Imai Y, Kuba K, Rao S, Huan Y, Guo F, Guan B, Yang P, Sarao R, Wada T, Leong-Poi H, Crackower MA, Fukamizu A, Hui CC, Hein L, Uhlig S, Slutsky AS, Jiang C, Penninger JM. Angiotensin-converting enzyme 2 protects from severe acute lung failure. Nature. 2005 — View Citation
Li F, Li W, Farzan M, Harrison SC. Structure of SARS coronavirus spike receptor-binding domain complexed with receptor. Science. 2005 Sep 16;309(5742):1864-8. — View Citation
Zhang H, Penninger JM, Li Y, Zhong N, Slutsky AS. Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target. Intensive Care Med. 2020 Apr;46(4):586-590. doi: 10.1007/s00134-020-05985-9. Epub 202 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Efficacy of captopril nebulization addition to standard of care compared to standard of care. | To assess determine the efficacy of captopril nebulization addition to standard of care compared to standard of care in term of 14-day ventilation free survival | 14 Days |
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