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Intravenous Infusions of Stem CellsWiki

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drug2951 Training video on anxiety, fear and loneliness in the COVID-19 environment. Wiki 1.00

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D045169 Severe Acute Respiratory Syndrome NIH 0.05
D018352 Coronavirus Infections NIH 0.04

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There is one clinical trial.

Clinical Trials


1 Efficacy of Intravenous Infusions of Stem Cells in the Treatment of COVID-19 Patients

Stem cell therapy has emerged as a revolutionary treatment for diseases that were considered untreatable only a few years ago. Umbilical cord-derived mesenchymal stem cells (UCMSCs) have been shown to repair damaged liver, kidney, heart, pancreas, skin, cartilage, and cornea in animal models and several human trials. In addition to cellular replacement through regeneration, UCMSCs mediate through paracrine signaling pathways resulting in immune modulation. Clinical manifestations of coronavirus disease 2019 (COVID-19), are believed to arise from septic shock and cytokine storm that cause acute respiratory dysfunction and acute cardiac injury. There is presently no cure for the COVID-19 viral disease; however, multi-treatment strategies are being examined. During the past two months, four reports were published that suggest, mesenchymal stem cells (MSCs), owing to their powerful immunomodulatory ability, may prevent the cytokine storm and thus reduce the COVID-19 related morbidity. All studies reported that COVID-19 patients responded favorably to MSCs therapy. These reports, taken together with the previous successes of stem cell therapy in animal models, the investigators, a seven-institution consortium, propose to explore the efficacy of UCMSC treatment in COVID-19 patients at Jinnah hospital, Lahore. The investigators propose to administer UCMSCs in patients with acute pulmonary inflammation due to COVID-19 infection with moderate to severe symptoms. In the first cohort of 15 patients, UCMSCs will be administered with three intravenous infusions of 500,000 UCMSCs per Kg body weight each on days 1, 3, and 5. The second group of five patients serving as control will only receive standard treatment. During the 30-day post-infusion period, a battery of tests will be performed to evaluate the safety and efficacy of the UCMSCs treatment. In parallel, the investigators propose a comparative study to determine COVID-19 viral count by quantitative real-time PCR and through viral coat protein ELISA, developed in the investigator advisor lab (Dr. Tauseef Butt, Progenra Inc. Philadelphia, USA) with the ultimate objective to locally developing a rapid diagnostic assay.

NCT04437823 Corona Virus Infection Biological: Intravenous Infusions of Stem Cells
MeSH:Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Description: Number of participants with significant side effects in stem cell treated group

Measure: Safety and efficacy assessment of infusion associated adverse events

Time: Day 01 to Day 30

Description: Assessment of Pneumonia improvement as a result of stem cell infusions

Measure: Chest Radiograph or Chest CT Scan

Time: Day 01 to Day 30

Secondary Outcomes

Description: Quantitative real-time PCR analysis for the evaluation of negative corona virus test results following stem cell treatment

Measure: COVID-19 Quantitative Real Time PCR

Time: Day 01 to Day 30

Description: Evaluation of organ function (Each organ system is assigned a value for 0 (normal) to 4 (highest degree of dysfunction))

Measure: Sequential Organ Failure Assessment (SOFA) Score

Time: Day 01 to Day 30

Description: Number of all mortalities within 30 days post first infusion

Measure: Rate of mortality

Time: Day 01 to Day 30

Description: Examination of improvement in the physiology of lungs after treatment

Measure: Clinical Respiratory Changes

Time: Day 01 to Day 30


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