There is one clinical trial.
Coronavirus disease (COVID-19) pandemic has started to affect Saudi Arabia and is expected to cause a lot of morbidities and many patients, especially the elderly, will require intensive care unit (ICU) support to survive as its lethality increases with the increasing age. Development of a vaccine by pharmaceutical companies like Roche and antibody concentrates from convalescent patients' plasma by Takeda will take 10-12 months to complete, and we speculate that it will be overwhelmingly expensive and limited in supply. We are presenting this urgent proposal to use the convalescent plasma to save the lives of severely affected COVID-19 patients. Most of the logistic support is already available in MOH Saudi Arabia, and it will be a cheap and quick technique based on the time-tested principles of passive immunization which is supported by the most recent data from China. We are proposing to test the therapeutic potential of convalescent plasma (from patients who have fully recovered from COVID-19) in treating patients with serious COVID-19 disease or those who are at risk of developing a serious disease based on their comorbidities profile. Convalescent plasma could provide our first-line defense for people with Covid-19, especially those who are older and at a much higher risk for complications. Amid the COVID-19 pandemic, with no available vaccine or proven antiviral drug, antibodies from recovering patients could provide a "stopgap" measure to help in controlling the pandemic effects on health and economy. We plan to recruit at least 40 consenting donors and patients. Non-consenting patients will serve as controls.
Description: number of days in ICUMeasure: ICU length of stay Time: Time from transfer into ICU to time of transfer out from ICU, Up to 12 weeks.
Description: reporting adverse events associated with transfusion as per transfusion medicine guidelines.Measure: Safety of convalescent plasma & Serious adverse reactions. Time: time from signing consent to one month after transfusion, Up to 12 weeks.
Description: number of days patient spend on ventilator.Measure: Number of days on mechanical ventilation Time: Time from intubation to time of extubation, Up to 12 weeks.
Description: the death rate in 30 days after signing consentMeasure: 30 days of mortality Time: 30 days from signing consent Up to 12 weeks.
Description: number of days to symptoms resolution and COVID 19 negative PCR ( by NP swap)Measure: Days to clinical recovery . Time: time from signing consent to recovery,Up to 12 weeks.
Data processed on January 01, 2021.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.Drug Reports MeSH Reports HPO Reports