Autologous Stromal Vascular Fraction of Cells for Treatment of Knee Articular Cartilage Dystrophy

NCT02827851 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2017-07-21

No results posted yet for this study

Summary

Stromal vascular fraction of cells (SVF) will be extracted from lipoaspirate by enzymatic digestion. SVF will be administered in a single dose intraarticularly 4 weeks after arthroscopic debridement. All patients will receive cell therapy.This is a single arm study with no control.

Conditions

Interventions

PROCEDURE

Liposuction

OTHER

SVF isolation

SVF will be isolated according to patent pending technology based on enzymatic digestion, washing and concentration of cell pellet in 5 ml of Hartmann's solution.

OTHER

Intraarticular administration of autologous SVF

Sponsors & Collaborators

  • Orenburg Regional Clinical Blood Donor Center

    collaborator UNKNOWN
  • Central Clinical Hospital w/Outpatient Health Center of Business Administration for the President of Russian Federation

    lead OTHER_GOV

Principal Investigators

  • Ilya I Eremin, MD, PhD · Federal State Budgetary Institution "Central Clinical Hospital with Outpatient Health Center" of the Business Administration for the President of the Russian Federation; Center for Biomedical Technologies

  • Rinat G Gilmutdinov, MD, PhD · Orenburg Regional Clinical Donor Blood Center

  • Sergey I Gilfanov, MD, PhD, Prof · Federal State Budgetary Institution "Central Clinical Hospital with Outpatient Health Center" of the Business Administration for the President of the Russian Federation

  • Andrey A Averyanov, MD, PhD · Orenburg Regional Clinical Hospital

  • Vadim A Kopylov, MD, PhD · Orenburg City Clinical Hospital #4

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2018-05-31
Completion
2018-11-30

Countries

  • Russia

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02827851 on ClinicalTrials.gov