COVID 19 Clinical Trial
Official title:
Does Therapeutic Plasma Exchange Have A Role in Resistant Cytokine Storm State Of COVID-19 Infection?
Verified date | April 2022 |
Source | Alexandria University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This research is planned to illustrate the efficacy of Therapeutic Plasma Exchange (TPE) treatment in COVID-19 patients with resistant cytokine storm state.
Status | Completed |
Enrollment | 10 |
Est. completion date | January 20, 2021 |
Est. primary completion date | December 29, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - COVID-19 positive patients (confirmed by PCR) with cytokine storm state who will not improve after two doses of tocilizumab. - Criteria of failure (resistance) to tocilizumab: 1. Persistent high IL-6 and CRP. 2. Persistent worsening of respiratory symptoms ( dyspnea, tachypnea, increased oxygen (O2) requirements or even need for mechanical ventilation). 3. Partial arterial pressure of oxygen to fractional inspired concentration of oxygen (PaO2/FiO2) ratio < 150. 4. Persistent fever (?38.5°C) despite normal procalcitonin level. Exclusion Criteria: - Refractory septic shock: ( It is defined according to surviving sepsis campaign as the presence of hypotension with end organ dysfunction requiring high dose vasopressor support often greater than 0.5 µg/kg/min norepinephrine or equivalent). |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Medicine, Alexandria university, Egypt | Alexandria |
Lead Sponsor | Collaborator |
---|---|
Alexandria University |
Egypt,
Adeli SH, Asghari A, Tabarraii R, Shajari R, Afshari S, Kalhor N, Vafaeimanesh J. Therapeutic plasma exchange as a rescue therapy in patients with coronavirus disease 2019: a case series. Pol Arch Intern Med. 2020 May 29;130(5):455-458. doi: 10.20452/pamw.15340. Epub 2020 May 7. — View Citation
Bassi E, Park M, Azevedo LC. Therapeutic strategies for high-dose vasopressor-dependent shock. Crit Care Res Pract. 2013;2013:654708. doi: 10.1155/2013/654708. Epub 2013 Sep 15. Review. — View Citation
Chan JF, Yuan S, Kok KH, To KK, Chu H, Yang J, Xing F, Liu J, Yip CC, Poon RW, Tsoi HW, Lo SK, Chan KH, Poon VK, Chan WM, Ip JD, Cai JP, Cheng VC, Chen H, Hui CK, Yuen KY. A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. Lancet. 2020 Feb 15;395(10223):514-523. doi: 10.1016/S0140-6736(20)30154-9. Epub 2020 Jan 24. — View Citation
Channappanavar R, Perlman S. Pathogenic human coronavirus infections: causes and consequences of cytokine storm and immunopathology. Semin Immunopathol. 2017 Jul;39(5):529-539. doi: 10.1007/s00281-017-0629-x. Epub 2017 May 2. Review. — View Citation
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. — View Citation
Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, Xia J, Yu T, Zhang X, Zhang L. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507-513. doi: 10.1016/S0140-6736(20)30211-7. Epub 2020 Jan 30. — View Citation
Kalaiyarasu S, Kumar M, Senthil Kumar D, Bhatia S, Dash SK, Bhat S, Khetan RK, Nagarajan S. Highly pathogenic avian influenza H5N1 virus induces cytokine dysregulation with suppressed maturation of chicken monocyte-derived dendritic cells. Microbiol Immunol. 2016 Oct;60(10):687-693. doi: 10.1111/1348-0421.12443. — View Citation
Patel P, Nandwani V, Vanchiere J, Conrad SA, Scott LK. Use of therapeutic plasma exchange as a rescue therapy in 2009 pH1N1 influenza A--an associated respiratory failure and hemodynamic shock. Pediatr Crit Care Med. 2011 Mar;12(2):e87-9. doi: 10.1097/PCC.0b013e3181e2a569. — View Citation
Ruan Q, Yang K, Wang W, Jiang L, Song J. Clinical predictors of mortality due to COVID-19 based on an analysis of data of 150 patients from Wuhan, China. Intensive Care Med. 2020 May;46(5):846-848. doi: 10.1007/s00134-020-05991-x. Epub 2020 Mar 3. Erratum in: Intensive Care Med. 2020 Apr 6;:. — View Citation
Singhal T. A Review of Coronavirus Disease-2019 (COVID-19). Indian J Pediatr. 2020 Apr;87(4):281-286. doi: 10.1007/s12098-020-03263-6. Epub 2020 Mar 13. Review. — View Citation
Sun D, Li H, Lu XX, Xiao H, Ren J, Zhang FR, Liu ZS. Clinical features of severe pediatric patients with coronavirus disease 2019 in Wuhan: a single center's observational study. World J Pediatr. 2020 Jun;16(3):251-259. doi: 10.1007/s12519-020-00354-4. Epub 2020 Mar 19. — View Citation
Ye Q, Wang B, Mao J. The pathogenesis and treatment of the 'Cytokine Storm' in COVID-19. J Infect. 2020 Jun;80(6):607-613. doi: 10.1016/j.jinf.2020.03.037. Epub 2020 Apr 10. Review. — View Citation
Zhang L, Zhai H, Ma S, Chen J, Gao Y. Efficacy of therapeutic plasma exchange in severe COVID-19 patients. Br J Haematol. 2020 Aug;190(4):e181-e183. doi: 10.1111/bjh.16890. Epub 2020 Jun 12. — View Citation
* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | mortality | Number of patients deaths of the total of patients included | 28 day | |
Secondary | the mean time with oxygen therapy | to calculate the mean time with oxygen therapy | through study completion, and average of 1 month | |
Secondary | the mean time with Non-invasive mechanical ventilation | to calculate the mean time with Non-invasive mechanical ventilation | through study completion, and average of 1 month | |
Secondary | the mean time of intubation | to calculate the mean time of intubation | through study completion, and average of 1 month | |
Secondary | respiratory function parameters | To calculate the mean of PaO2/FiO2 | through study completion, and average of 1 month | |
Secondary | respiratory function parameters | To calculate the mean of levels of oxygen saturation | through study completion, and average of 1 month | |
Secondary | radiological lung extension | to evaluate the lung extension of pneumonia | through study completion, and average of 1 month | |
Secondary | mean duration of hospitalization and ICU use | Days of hospitalization in survivors and/or days at ICU throughout the study | through study completion, and average of 1 month | |
Secondary | the requirement of additional organ support | Percentage of patients with dialysis | through study completion, and average of 1 month | |
Secondary | the levels of IL-6 | To evaluate the effect of TPE on the serum levels of inflammatory markers | through study completion, and average of 1 month | |
Secondary | Incidence of adverse events | To calculate the number of adverse events in patients with COVID-19 treated with TPE | through study completion, and average of 1 month | |
Secondary | time to reverse-transcriptase polymerase chain reaction (RT-PCR) virus negativity | To evaluate the time to RT-PCR virus negativity | through study completion, and average of 1 month | |
Secondary | the levels of CRP | To evaluate the effect of TPE on the serum levels of inflammatory markers | through study completion, and average of 1 month | |
Secondary | the levels of procalcitonin (PCT) | To evaluate the effect of TPE on the serum levels of inflammatory markers | through study completion, and average of 1 month | |
Secondary | levels of D-dimer | To evaluate the effect of TPE on the serum levels of inflammatory markers | through study completion, and average of 1 month | |
Secondary | levels of ferritin | To evaluate the effect of TPE on the serum levels of inflammatory markers | through study completion, and average of 1 month |
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