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Russian Clinical Trial of Mesenchymal Cells in Patients With Septic Shock and Severe Neutropenia

Russian Single-center Open Randomized Clinical Trial of the Impact of Mesenchymal Stromal Cells Therapy on Organ Dysfunction and 28-day Mortality in Patients With Septic Shock and Severe Neutropenia.

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01849237
Enrollment
30
Registered
2013-05-08
Start date
2012-12-31
Completion date
2015-05-31
Last updated
2013-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neutropenia After Chemotherapy in Oncohematological Patients, Neutropenia in Patients With Aplastic Anemia, Nonchemotherapy Drug-induced Neutropenia, Septic Shock

Keywords

Mesenchymal Stromal Cells, Septic Shock, Neutropenia, Procalcitonin, Interleukin-6, Interleukin-10, C-reactive protein, Survival, Organ dysfunction

Brief summary

Septic shock remains a significant clinical problem associated with high rates of mortality among neutropenic patient despite antimicrobial therapy and supportive care. Recently, mesenchymal stromal cells (MSC) have demonstrated remarkable potential effect in sepsis. MSC treatment significantly reduced mortality in septic mice receiving appropriate antimicrobial therapy. MSCs reduced systemic inflammatory cytokine levels in mice, down-regulated of inflammation and inflammation-related genes (such as interleukin-10, interleukin-6). Bacterial clearance was greater in MSC-treated mice. Thus, MSCs have beneficial effects on experimental sepsis and suggest that MSСs-therapy may be an effective adjunctive treatment to reduce sepsis-related mortality. The safety of MSCs is proved by Graft-versus-host disease treatment MSCs in patients after bone marrow transplantation. This study hypothesis is that MSCs reduce organ dysfunction/injury, systemic inflammation and mortality in patients with septic shock and severe neutropenia. The main goal of the study is to evaluate the impact of MSCs therapy on organ dysfunction/injury, systemic inflammation and 28-day mortality in patients with septic shock and severe neutropenia. All patients will be randomized in two groups: control group (standard treatment of septic shock) and MSCs-group (standard treatment of septic shock + MSCs infusion of 1-2 millions/kg/ day).

Detailed description

All activities related to this human subjects research have been guided by ethical principles and have been reviewed and approved Federalwide Assurance National Ctr for Hematology, FWA00006482. The goal of the trial is to evaluate plasma concentration of proinflammatory cytokine interleukin-6 and the antiinflammatory cytokine interleukin-10, plasma levels of blood creatinine, bilirubin, procalcitonin, C-reactive protein. Then we will evaluate requirement for renal replacement therapy, requirement for mechanical ventilation or non-invasive mechanical ventilation, pulmonary function-coefficient, partial oxygen pressure arterial blood level, electrocardiograms, Kaplan - Meier curve,28-days mortality.

Interventions

GENETICMesenchymal stromal cells

MSCs intravenous infusion of 1-2 millions/kg/day will be performed not more than 10 hs after onset of septic shock in patients with severe neutropenia(≤ 1x10\^9/l).

DRUGStandard therapy of septic shock

Antibiotic therapy Fluid therapy Vasopressors Inotropic therapy Steroids

Sponsors

National Research Center for Hematology, Russia
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
17 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

septic shock ≤10 hs after onset of septic shock severe neutropenia(≤ 1 10\^9/l) Patients ≥17 years Signed Informed Consent to treatment

Exclusion criteria

oncohematological patients with resistance to chemotherapy Unsigned Informed Consent to treatment Age \>75 years; Pregnancy

Design outcomes

Primary

MeasureTime frame
mortality28 days

Secondary

MeasureTime frameDescription
Evaluation of MSC therapy effects on organ dysfunctionAt Baseline and at day 2,3,7,14,21,281. Liver: levels of serum total bilirubin, transaminases, lactate dehydrogenase, plasma protrombin level 2. Pancreas: amylase level 3. Renal: number of hemodialysis/ hemodiafiltration, blood urea and creatinine levels 4. Pulmonary: requirement for mechanical ventilation or non-invasive mechanical ventilation, pulmonary function-coefficient, partial oxygen pressure arterial blood level 5. Cardiac: requirement for vasopressors, main parameters obtained from Transpulmonary Thermodilution- Systemic Vascular Resistance Index ( SVRI ), Cardiac Output (CO)
Evaluation of MSC therapy effects on systemic inflammatory parametersAt Baseline and at day 2,3,7,14,21,28plasma concentration of proinflammatory cytokine IL-6 and the antiinflammatory cytokine IL-10, concentration of procalcitonin, C-reactive protein Fibrinogen level, lactate level , the factor XII-dependent fibrinolytic activity blood routine examination
Evaluation of MSC therapy effects on septic shock reversalAt Baseline and at day 2,3,7,14,21,28SOFA score

Countries

Russia

Contacts

Primary ContactGennady Galstyan, MD PhD
gengalst@gmail.com+7(495)6124859

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026