Official Title
Two-treatment,Randomized, Controlled, Multicenter Clinical Trial to Assess the Safety and Efficacy of Intravenous Administration of Expanded Allogeneic Adipose Tissue Adult Mesenchymal Stromal Cells in Critically Ill Patients COVID-19
Brief Summary

The investigational medicinal product consists of expanded allogeneic mesenchymal stromal cells derived from adipose tissue and administered intravenously. The objective of this project is to evaluate the safety and efficacy of the administration of expanded allogeneic adipose tissue adult mesenchymal stem cells, in patients infected with SARS-COV-2 with COVID-19 type complications.

Suspended
COVID
Respiratory Distress Syndrome

Drug: Allogeneic and expanded adipose tissue-derived mesenchymal stromal cells

Two serial doses of 1.5 million adipose-tissue derived mesenchymal stem cells per kg

Eligibility Criteria

Inclusion Criteria:

- Patients of both sexes.

- Over 18 years.

- Confirmation of SARS-COV-2 infection by RT-PCR in respiratory sample.

- Respiratory failure requiring intubation and connection to mechanical ventilation,
secondary to SARS-CoV-2 infection.

- Criteria for acute respiratory distress: acute bilateral alveolar-interstitial
infiltrate not compatible with left ventricular failure (demonstrated with ultrasound
or hemodynamic parameters), sudden onset, and blood gas compromise with a PaO2 / FiO2
ratio <200 mm-Hg.

- Women of childbearing potential should have a negative urine pregnancy test performed
at the time of study enrollment.

- Written or verbal informed consent from the patient, family member or legal
representative.

Exclusion Criteria:

- Any other cause of acute respiratory distress not attributable to SARS-Cov-2.

- RT-PCR of SARS-Cov-2 negative.

- Multi-organ failure (more than three organs)

- Severe respiratory failure requiring extracorporeal support (ECMO) Grave Moderate
severe COPD requiring chronic home oxygen therapy, need for prior home oxygen therapy
for any reason.

- Pregnancy, lactation and women of childbearing age but who do not take effective
contraceptive measures.

- Active tumor disease.

- Previous immunosuppressive treatment.

- Allergy or hypersensitivity to the administered products.

- History of deep vein thrombosis or pulmonary embolism in the last 3 years.

- Participation in other clinical trials during the 3 months prior to the initial visit.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
Spain
Locations

Fundacion Jimenez Diaz
Madrid, Spain

Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz
NCT Number
MeSH Terms
Respiratory Distress Syndrome
Respiratory Distress Syndrome, Newborn