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Mesenchymal stem cells (MSCs) are of potential help in acute respiratory distress syndrome (ARDS), due to their anti-inflammatory properties.
The investigators will analyze the effect of 3 iterative infusions of ex vivo expanded Wharton's Jelly MSCs (total dose 2.10^6/kg) in patients with ARDS due to COVID19, who require mechanical ventilation.
This study is designed to analyze the impact of Wharton's Jelly Mesenchymal Stem Cells on moderate to severe ARDS due to COVID19 in adult patients who require mechanical ventilation. It is a Phase IIa double-blind randomized controlled trial.
30 patients are planned.
Patients will be randomized and will receive, with the conventional treatment recommended to treat ARDS:
Either Wharton's Jelly MSCs in a solution of albumin 4% (40% of final volume), NaCl 0,9% (50% of the final volume) et ACD formule A (10% of the final volume) . Treatment will be administered intravenously during 10 minutes following that scheme:
Either a placebo, which contains the same solution of albumin, NaCl 0.9% and ACD without cells. The volume will be of 75 ml, infused in 10 minutes.
The main objective is to investigate efficacy of WJ-MSCs, compared to a placebo, on respiratory function evolution during the first 14 days of study treatment in patients with SARS-CoV-2 related moderate to severe ARDS.
Secondary objectives are to assess the effect of WJ-MSC, compared to placebo, in patients with SARS-CoV-2 related moderate to severe ARDS, on:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MSC Arm | Experimental | Ex vivo expanded Wharton's Jelly derived mesenchymal stem cells will be infused at day 0, day 3 and day 5 (+/- 1 day), in patients with moderate to severe ARDS with a mechanical ventilation. day 0: 1.10^6 MSC/kg day 3: 0.5. 10^6 MSC/kg day 5: 0.5 . 10^6 MSC/kg |
|
| Placebo Arm | Placebo Comparator | Only the vehicle solution, without MSCs, containing albumin 4% , NaCl 0,9% and ACD will be injected to patients at day 0, 3 and 5 (+/-1 day). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ex vivo expanded Wharton's Jelly Mesenchymal Stem Cells | Biological | Ex vivo expanded Wharton's Jelly derived mesenchymal stem cells will be infused at day 0, day 3 and day 5 (+/- 1 day), in patients with moderate to severe ARDS with a mechanical ventilation. day 0: 1.10^6 MSC/kg day 3: 0.5. 10^6 MSC/kg day 5: 0.5 . 10^6 MSC/kg |
| Measure | Description | Time Frame |
|---|---|---|
| PaO2 / FiO2 ratio | The primary endpoint is the percentage of patients with a PaO2/FiO2 ratio > 200 at D10 of treatment with MSC-GW or placebo. | day 10 |
| Measure | Description | Time Frame |
|---|---|---|
| respiratory function evolution | The evolution of the PaO2/FiO2 ratio between Day 0 (or Day 1) and Day 14 of treatment with MSC-GW or placebo is a secondary endpoint. | between Day 0 (or Day 1) and Day 14 of treatment |
| respiratory assistance |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Antoine KIMMOUN, MD, PhD | Central Hospital, Nancy, France | Principal Investigator |
| Sébastien GIBOT, MD, PhD | Central Hospital, Nancy, France | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nancy University Hospital | Vandœuvre-lès-Nancy | 54500 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 37706025 | Derived | Pochon C, Laroye C, Kimmoun A, Reppel L, Dhuyser A, Rousseau H, Gauthier M, Petitpain N, Chabot JF, Valentin S, de Carvalho Bittencourt M, Peres M, Aarnink A, Decot V, Bensoussan D, Gibot S. Efficacy of Wharton Jelly Mesenchymal Stromal Cells infusions in moderate to severe SARS-Cov-2 related acute respiratory distress syndrome: a phase 2a double-blind randomized controlled trial. Front Med (Lausanne). 2023 Aug 29;10:1224865. doi: 10.3389/fmed.2023.1224865. eCollection 2023. |
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| ID | Term |
|---|---|
| D007249 | Inflammation |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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Phase IIa double-blind randomized controlled trial
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| Placebo | Biological | Only the vehicle solution, without MSCs, containing albumin 4% , NaCl 0,9% and ACD will be injected to patients at day 0, 3 and 5 (+/-1 day). |
|
The effect of WJ-MSC on respiratory assistance is evaluated by the proportion of days without invasive respiratory assistance during the hospital stay and maximum on Day 28 (number of days without invasive respiratory assistance / number of hospital days fixed at day 28)
| between day 0 (or 1) and day 28 (or last day of hospitalization if before day 28) |
| organ failures 1 | Difference in sequential organ failure assessment score (SOFA score), grading 0 (best) to 4 (worst), between Day 5-Day 0 and D14-Day 0 | Day 0 to day 14 |
| organ failures 2 | number of days without extra-renal treatment / number of hospital days fixed at day 28 | day 0 to day 28 |
| organ failures 3 | number of days without vasopressor support | day 0 to day 28 |
| duration of intensive care | The duration of stay in intensive care unit | day 0 to 90 |
| Cause of death | Cause of death during the stay in intensive care unit and during the hospital stay, on Day 28 and Day 90 | day 0 to 90 |
| respiratory morbidity (TDM, functional respiratory measures) | respiratory morbidity on Day 90 | day 90 |
| viral load | The evolution of the viral load is evaluated by RT PCR SARS-Cov-2 monitoring on a nasopharyngeal swab (or any other sample) at diagnosis, at Day 7, Day 14, Day 21, Day 28 or on the last day of hospitalisation | day 0 to day 28 (or last day of hospitalization if before day 28) |
| Anti-HLA antibody rate | - The anti-HLA antibody rate measured on Day 0 (before initiating treatment), on Day 28 and on Day 90 | day 0 to day 90 |
| immediate hypersensitivity reactions | The occurrence of immediate hypersensitivity reactions (chills, hyperthermia associated with hypotension) within 4 to 6 hours of the WJ MSC or placebo infusion. | day 0, day 3, day 5 (+/- 1day) |
| thromboembolic adverse events 1 | The thromboembolic risks monitored biologically by routinely daily monitoring of hemostasis (TP, TCA, Fibrinogen, D-dimers) | day 0 to day 14 |
| thromboembolic adverse events 2 | daily monitoring of transthoracic echocardiography | day 0 to day 14 |
| infectious adverse events | blood cultures in case of T° > 38,5°C | day 0 to day 14 |