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WithdrawnNCT04850469Updated Jun 15, 2022

Study of MSC-Exo on the Therapy for Intensively Ill Children

An observational study in Sepsis and Critical Illness, sponsored by Children's Hospital of Fudan University. Withdrawn at 1 site in China. Open to participants aged 29 Days to 18 Years. Per ClinicalTrials.gov, last updated 2022-06-15.

Sponsored by Children's Hospital of Fudan University · Observational

Why this study was withdrawn
Lacking of funding
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
29 Days to 18 Years
Sex
All
01

Study summary

At present, a number of projects related to MSCs have been approved for graft-versus-host disease, myocardial infarction, Crohn's disease and other diseases, indicating a strong therapeutic potential of MSCs. However, the efficacy of MSC-Exo for severely infected children is not fully evaluated. In our study, patients who met the inclusion criteria will be divided into trial group and control group. Clinical and demographic data, as well as treatment outcome will be collected from the electronic health record. This study will evaluate the application and therapeutic effect of MSC-Exo in severely infected children, and determine the Optimal dosage and infusion.

Read the detailed description

Mesenchymal stem cells (MSCs) are pluripotent stem cells with high self-renewal ability and multidirectional differentiation potential. studies revealed that local or systemic administration of mesenchymal stem cell-derivrd exosomes (MSC-Exo) efficiently suppressed detrimental immune response in inflamed tissues and promoted survival and regeneration of injured parenchymal cells. European Union countries have written MSCs into treatment guidelines for refractory graft-versus-host disease.

In China, the technology for isolation, in vitro culture and expansion of MSCs is already mature. With further research on the therapeutic efficacy of MSC-Exo and the development of clinical trials, it is expected to become a treatment for severe illness.

A predictable infection plan is going to be widely used in clinics to provide individualized treatment for patients, improve the prognosis of patients and improve the quality of life.

The investigators intend to enroll all children who were hospitalized in pediatric intensive care unit PICU of Children's Hospital of Fudan University from January 2022 to December 2023. Children with a PICU length of day less than 48h will be excluded.

02

Conditions studied

  • Sepsis
  • Critical Illness

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Keywords

  • Sepsis
  • Critical Illness
  • Mesenchymal Stem Cell Derived Exosomes
03

In context

Critical Illness

1,881 studies on the registry are indexed under Critical Illness; 462 are open to participants now.

Browse Critical Illness studies →

Lead sponsor

Children's Hospital of Fudan University is the lead sponsor of 262 studies on the registry; 92 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
29 Days to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All children hospitalized in PICU of Children's Hospital of Fudan University from January 2022 to December 2023

Inclusion criteria

  • children hospitalized in PICU of Children's Hospital of Fudan University

Exclusion criteria

Exclusion Criteria:

  • discharge within 48 hours
  • patients without informed consent
  • incomplete clinical and demographic data
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No

Groups and cohorts

  • trial group

    Mesenchymal Stem Cell-Derived Exosomes

  • control group

    conventional treatment

06

What researchers measure

Primary outcomes

  1. The death rate of children

    The death rate of children in 28 days after their discharged from PICU

    Time frame: within 28 days after they discharged from PICU

  2. Marshall Multiple Organ Dysfunction Score

    The Marshall Multiple Organ Dysfunction Score (MODS) assesses the same six organ systems using slightly different values for four grades of organ dysfunction. The total score, ranging from 0 to 24, arises from the sum of all single organ scores using the first measured value of the day. Intervals for the most abnormal value of each variable were constructed on a scale from 0 to 4 so that a value of 0 represented essentially normal function and was associated with an ICU mortality rate of \< 5%, whereas a value of 4 represented marked functional derangement and an ICU mortality rate of \> or = 50%.

    Time frame: Within 3 to 15 days after the start of treatment

  3. the APPS score

    The APPS is a 9-point score that is calculated by measuring the age, PaO2/FIO2 ratio, and plateau pressure at 24 h after the patient is diagnosed with moderate to severe ARDS and counting each one to 1-3. Since many variables are not needed for calculations, clinicians can easily predict the in-hospital mortality of mechanically ventilated patients with moderate to severe ARDS patients at bedside.

    Time frame: Within 3 to 15 days after the start of treatment

Secondary outcomes

  1. length of stay in PICU

    Time from PICU admission to discharge

    Time frame: up to 28 days

07

Study locations

1 site
  • Children's Hospital of Fudan University
    Shanghai, Shanghai, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 15, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04850469
Lead sponsor
Children's Hospital of Fudan University
Responsible party
Sponsor
First posted
Apr 20, 2021
Start date
Sep 1, 2022 (estimated)
Primary completion
Dec 31, 2023 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Jun 15, 2022

Study contacts

Guoping Lu, Doctor
principal investigator · Children's Hospital of Fudan University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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