CovidResearchTrials by Shray Alag


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Therapeutic Plasma ExchangeWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (3)


Name (Synonyms) Correlation
drug2823 TY027 Wiki 0.71
drug7 0.9% Saline Wiki 0.71
drug2471 Ruxolitinib Wiki 0.24

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D013577 Syndrome NIH 0.07
D018352 Coronavirus Infections NIH 0.03

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There are 2 clinical trials

Clinical Trials


1 Interventional Study to Evaluate the Efficacy of Therapeutic Plasma Exchange (TPE) Alone or in Combination With Ruxolitinib in COVID-19 Positive Patients With PENN Grade 2, 3, 4 Cytokine Released Syndrome (CRS)

This protocol will evaluate the efficacy of Therapeutic Plasma Exchange alone or in combination with ruxolitinib in COVID positive patients with PENN grade 2, 3, 4 cytokine release syndrome. It is hypothesized that dual intervention of acute apheretic depletion of cytokines and concomitant suppression of production will produce superior amelioration of the cytokine load and to help to prevent cytokine load rebound. This protocol is envisioned as a pilot study (n=20) for hypothesis generation for future investigation.

NCT04374149 Cytokine Release Syndrome COVID19 Procedure: Therapeutic Plasma Exchange Drug: Ruxolitinib
MeSH:Syndrome

Primary Outcomes

Description: Defined as greater than or equal to 33% decrease in cytokine load in one-third or more participants

Measure: Overall Response Rate

Time: 14 days

2 "PLEXIT - Therapeutic Plasma Exchange (TPE) for Covid-19 Cytokine Release Storm (CRS), a Retrospective Propensity Matched Control Study"

Background: investigators have seen recently from experience in Western countries with best health care systems that pandemics cannot be managed in hospitals. Investigators have seen ICUs crowded to capacity, healthcare workers being exposed and going to quarantine or dying after exposure to large doses of viral inoculums. Investigators recommend that institutions should register for Clinical trials and consider emergency use of TPE. In Pandemics, time is of essence to avoid mortality by intervening early with available evidence, preferably as part of clinical trial. Scientific rationale: Beyond supportive care, there are currently no proven treatment options for coronavirus disease (COVID-19) and related pneumonia, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). However, literature review has shown that most common cause of death in severe SARS-COV-2 is Cytokine release syndrome and Hemophygocytic Lymphohistocytosis (HLH). In this context, Investigators seek to treat patients who are sick enough to warrant hospitalization prior to the onset of overwhelming disease including a systemic inflammatory response, sepsis, and/or Acute Respiratory Distress Syndrome (ARDS).

NCT04485169 COVID-19 Cytokine Release Syndrome Procedure: Therapeutic Plasma Exchange

Primary Outcomes

Description: Death or recovery

Measure: Survival

Time: 28 days

Secondary Outcomes

Description: Duration of hospitalization in days

Measure: Duration of Hospitalization

Time: 28 days

Description: Time in days to achieve viral clearance

Measure: Timing of PCR negativity

Time: 28 days

Description: Time in days required to settle symptoms and laboratory parameters of CRS

Measure: Time to CRS resolution

Time: 28 days

Description: Complications secondary to use of TPE

Measure: Complications

Time: 28 days


No related HPO nodes (Using clinical trials)