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CompletedNCT02386163Updated Sep 10, 2015

Large-scale ex Vivo Expansion and Characterization of Two Kinds of MSC From Knee for Clinical Application

An observational study in Knee Injuries, sponsored by EMO Biomedicine Corporation. Completed at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2015-09-10.

Sponsored by EMO Biomedicine Corporation · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
6
Ages
20 Years and older
Sex
All
01

Study summary

According to many researches, mesenchymal stem cells (MSC) isolated from synovial membrane and infrapatellar fat pad have higher ex vivo proliferation capacity, multipotency and ability to undergo chondrogenesis.

Based on this concept, the investigators plan to get two removed tissues (synovial membrane and infrapatellar fat pad) from patients who have an operation of TKR (Total Knee Replacement). The investigators are going to isolate and expand MSC from these two tissues respectively, and then compare their characterization and potential for clinical application. In the other hand, the investigators plan to build techniques and procedures which comply with "Good Tissue Practices (GTP)".

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Conditions studied

  • Knee Injuries

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03

In context

Knee Injuries

249 studies on the registry are indexed under Knee Injuries; 48 are open to participants now.

This study's enrollment of 6 is below the median of 90 across 79 observational studies indexed under Knee Injuries.

Browse Knee Injuries studies →

Lead sponsor

EMO Biomedicine Corporation is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

For patients who have an operation of total knee replacement.

Inclusion criteria

Patient who have an total knee replacement surgery

Exclusion criteria

Exclusion Criteria:

Patient who don't sign the agreement

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
6 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Interventions

  • BiologicalMSC from synovial membrane and infrapatellar Fat Pad
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What researchers measure

Primary outcomes

  1. Compare MSCs from synovial membrane and infrapatellar fat pad

    Comparison items include doubling time, phenotype, chondrogenesis and biological activity.

    Time frame: 2 months

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Study locations

1 site
  • Far Eastern Memorial Hospital
    New Taipei City, 220, Taiwan
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02386163
Lead sponsor
EMO Biomedicine Corporation
Collaborators
Far Eastern Memorial Hospital
Responsible party
Sponsor
First posted
Mar 11, 2015
Start date
May 2014
Primary completion
Aug 2015
Completion
Aug 2015
Last update
Sep 10, 2015

Study contacts

Chih-Hung Chang, MD, Ph.D
principal investigator · Far Eastern Memorial Hospital
Shing-Mou Lee
study chair · EMO Biomedicine Corp.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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