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Mesenchymal Stem Cells for Multiple Organ Dysfuntion Syndrome After Surgical Repaire of Acute Type A Aortic Dissection

Primary Purpose

Multiple Organ Dysfunction Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
MSC
Sponsored by
Fujian Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Organ Dysfunction Syndrome

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Part 1:

  • Patients who are diagnosed with ATAAD and received emergency surgery with ascending aortic replacement combined with open placement of triple-branched stent graft
  • elder than 60 years old
  • Preoperative PaO2/FiO2 > 400mmHg, platelets ≥ 150*109/L, bilirubin < 20μmol/L, no hypotension (without vasoactive drugs), Glasgow Coma Score Scale = 15, creatine <110μmol/L

Part 2:

  • Patients who are diagnosed with ATAAD and received emergency surgery with ascending aortic replacement combined with open placement of triple-branched stent graft
  • Patients who have failure of at least 2 organs
  • Patients who meet the criteria as below:

sequential organ failure assessment score (SOFA) ≥ 10

Exclusion Criteria:

  • uncontrollable underlying disease life expectancy of less than 4 days history of long-term corticosteroid use during the past 6 months.
  • The pre-operative computer tomography angiography(CTA) demonstrate the visceral arteries are involved
  • pre-existing severe disease of any major organs

Sites / Locations

  • Department of Cardiovascular SurgeryRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Mesenchymal stem cell

Control

Arm Description

Patients in the MSC arm will be given MSC, i.v., 1000000 cells per kilogram of body weight.

Patients in the control arm will not be given MSC.

Outcomes

Primary Outcome Measures

survival after intervention
survival after intervention: comparing survival ratio in hospital(6 months post-intervention) between groups.
adverse events
short term adverse events such as anaphylactic reaction, embolism; long term adverse events, such as oncogenicity
sequential organ failure assessment score(SOFA)
Compare the change of sequential organ failure assessment score(SOFA) between groups.
interleukin-6
Compare the change of interleukin( IL)-6 between groups.

Secondary Outcome Measures

the effects on kidney function
the therapeutic effects in the improvement of kidney function, as indicated by Scr level.
the effects on liver function
the therapeutic effects in the improvement of liver function, as indicated by bilirubin levels.
the effects on lung function
the therapeutic effects in the improvement of lung function, as indicated by oxygenation index.
the effects on coagulation function
the therapeutic effects in the improvement of coagulation function, as indicated by blood platelet count.
the effects on central nervous system
the therapeutic effects in the improvement of coagulation function, as indicated by Glosgow coma score

Full Information

First Posted
May 29, 2018
Last Updated
June 16, 2019
Sponsor
Fujian Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03552848
Brief Title
Mesenchymal Stem Cells for Multiple Organ Dysfuntion Syndrome After Surgical Repaire of Acute Type A Aortic Dissection
Official Title
Mesenchymal Stem Cells for Multiple Organ Dysfuntion Syndrome After Surgical Repaire of Acute Type A Aortic Dissection: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
December 1, 2019 (Anticipated)
Study Completion Date
December 1, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fujian Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Multiple organ dysfunction syndrome (MODS) after surgical repaire for acute type A aortic dissection(ATAAD) is a life-threatening condition. In this study, patients who undergoing surgical repaire of ATAAD immdediately or presenting sever MODS after surgical repaire of acute type A aortic dissection will be treated with umbilical cord-derived mesenchymal stem cell.
Detailed Description
Multiple organ dysfunction syndrome(MODS) are common debilitating complications after surgical repaire for ATAAD. MODS is one of the chief causes of post-operative death for acute type A aortic dissection(ATAAD) patients, and it was reported that MODS accounted for more than half of the death after surgery for ATAAD. Despite recent advance in surgical technique, mortality rate remains high in such critical care conditions. In animal models, studies have demonstrated the beneficial effects of MSCs with respect to ischemia-reperfusion injury of heart, lungs, kidney, brains and livers. Several pilot studies have provided evidence that MSC may be effective in treating critically ill patients with traumatic brain injury, acute renal failure, or acute respiratory distress syndrome. Therefore, in the present pilot study, the investigators hypothesized that timely initiation of mesenchymal stem cells(MSC) will positively influence survival and biochemical indexesof patients with MODS after ascending aortic replacement combined with open placement of triple-branched stent graft for ATAAD. The trial contain two parts: Part one(prenvention scheme): to explore the safety and efficacy of umbilical cord-derived MSC, we will recruit patients who are diagnosed with ATAAD, and 8 patients will be administrated intervenously with MSC immediately after ascending aortic replacement combined with open placement of triple-branched stent graft while other 8 not. Then we will monitor their MODS related biochemical indexes, sequential organ failure assessment(SOFA) scores, comparing to those don't be treated with MSC. Phase two(treatment scheme): for patients presenting severe MODS(SOFA score≥10) after ascending aortic replacement combined with open placement of triple-branched stent graft, we will randomly use MSC to 8 of patients while other 8 not. Then we will monitor their MODS related biochemical indexes, SOFA scores, comparing to those don't be treated with MSC. The dosage of the MSC was determined on the basis of the previous clinical studies, which is 1000000 cells per kilogram of body weight and administrated intervenously .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Organ Dysfunction Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Part 1: totally 30 patient will be enrolled, and 15 patients will be given MSC immediately after ascending aortic replacement combined with open placement of triple-branched stent graft for ATAAD. Part 2: totally 30 patient will be enrolled, and 15 patients will be given MSC after onset of multiple organ dysfuntion syndrome after ascending aortic replacement combined with open placement of triple-branched stent graft for ATAAD.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mesenchymal stem cell
Arm Type
Experimental
Arm Description
Patients in the MSC arm will be given MSC, i.v., 1000000 cells per kilogram of body weight.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients in the control arm will not be given MSC.
Intervention Type
Biological
Intervention Name(s)
MSC
Intervention Description
MSC at a dose of 1000000 cells per kilogram of body weight will be given intravenously once every 4 days for 4 times
Primary Outcome Measure Information:
Title
survival after intervention
Description
survival after intervention: comparing survival ratio in hospital(6 months post-intervention) between groups.
Time Frame
Up to 6 month
Title
adverse events
Description
short term adverse events such as anaphylactic reaction, embolism; long term adverse events, such as oncogenicity
Time Frame
Up to 2 years
Title
sequential organ failure assessment score(SOFA)
Description
Compare the change of sequential organ failure assessment score(SOFA) between groups.
Time Frame
Up to 6 months
Title
interleukin-6
Description
Compare the change of interleukin( IL)-6 between groups.
Time Frame
Early 3 days
Secondary Outcome Measure Information:
Title
the effects on kidney function
Description
the therapeutic effects in the improvement of kidney function, as indicated by Scr level.
Time Frame
Up to 6 months
Title
the effects on liver function
Description
the therapeutic effects in the improvement of liver function, as indicated by bilirubin levels.
Time Frame
Up to 6 months
Title
the effects on lung function
Description
the therapeutic effects in the improvement of lung function, as indicated by oxygenation index.
Time Frame
Up to 6 months
Title
the effects on coagulation function
Description
the therapeutic effects in the improvement of coagulation function, as indicated by blood platelet count.
Time Frame
Up to 6 months
Title
the effects on central nervous system
Description
the therapeutic effects in the improvement of coagulation function, as indicated by Glosgow coma score
Time Frame
Up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Part 1: Patients who are diagnosed with ATAAD and received emergency surgery with ascending aortic replacement combined with open placement of triple-branched stent graft elder than 60 years old Preoperative PaO2/FiO2 > 400mmHg, platelets ≥ 150*109/L, bilirubin < 20μmol/L, no hypotension (without vasoactive drugs), Glasgow Coma Score Scale = 15, creatine <110μmol/L Part 2: Patients who are diagnosed with ATAAD and received emergency surgery with ascending aortic replacement combined with open placement of triple-branched stent graft Patients who have failure of at least 2 organs Patients who meet the criteria as below: sequential organ failure assessment score (SOFA) ≥ 10 Exclusion Criteria: uncontrollable underlying disease life expectancy of less than 4 days history of long-term corticosteroid use during the past 6 months. The pre-operative computer tomography angiography(CTA) demonstrate the visceral arteries are involved pre-existing severe disease of any major organs
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhihuang Qiu, M.D
Phone
86 13805065508
Email
qzhflm@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liangwan Chen, M.D
Organizational Affiliation
Union Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Cardiovascular Surgery
City
Fuzhou
State/Province
Fujian
ZIP/Postal Code
350001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liang-Wan Chen, M.D, Ph.D
Phone
86 13358255333
Email
daixiaofu719@hotmail.com
First Name & Middle Initial & Last Name & Degree
E Lin, M.D
Phone
86 13365912195
Email
1470054258@qq.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Mesenchymal Stem Cells for Multiple Organ Dysfuntion Syndrome After Surgical Repaire of Acute Type A Aortic Dissection

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