Autologous Micro-fragmented Adipose Tissue Injection for Knee Osteoarthritis

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03788265
Collaborator
(none)
60
1
1
60
1

Study Details

Study Description

Brief Summary

Knee osteoarthritis (OA) is characterized by loss of cartilage leading to instability, reduced range of motion, and functional limitations. Current treatment has various limitations so that alternative options to restore function and alleviate joint pain, with the ultimate goal of healing damaged articular cartilage are needed. Mesenchymal stem cells (MSCs) therapy has shown promising results. However, MSCs are limited by complex regulatory issues. Lipogems is a technique to harvest, process, and inject minimally manipulated adipose tissue through mild mechanical force. This procedure is enzyme free and requires no clonal expansion or manipulation. The goal of this study is to evaluate the possible benefits of reduced joint pain and increased joint functionality in patients with knee osteoarthritis after the injection of Lipogems.

Condition or Disease Intervention/Treatment Phase
  • Device: Lipogems
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Autologous Micro-fragmented Adipose Tissue Intra-articular Injection for Knee Osteoarthritis
Actual Study Start Date :
Jan 1, 2016
Anticipated Primary Completion Date :
Jan 1, 2020
Anticipated Study Completion Date :
Jan 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: injection

Device: Lipogems
harvest and inject micro-fragment adipose tissue

Outcome Measures

Primary Outcome Measures

  1. Change in Visual Analog Pain Scale (VAS) Over Time [Pre-op, then post-op: 1 month, 3 months, 6 months, 1 year, 2 years]

    Scaled pain score to assess change in a patient's knee pain over time. Pain level is marked on a 100 mm line with the 0 mm corresponding to "no pain" and the 100 mm corresponding to 10/10 pain. Using a ruler, the score is determined by measuring the distance (mm) on the 100 mm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100. The following cut points on the pain VAS have been recommended: no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm).

Secondary Outcome Measures

  1. Change in the knee injury and osteoarthritis score (KOOS) Over Time [Pre-op, then post-op: 1 month, 3 months, 6 months, 1 year, 2 years]

    Patient self-reported outcome measure to assess the patient's opinion about their knee and associated issues. KOOS consists of 5 subscales; Pain, other Symptoms, Function in daily living (ADL), Function in sport and recreation (Sport/Rec) and knee related Quality of life (QOL). Standardized answer options are given (5 Likert boxes) and each question gets a score from 0 to 4. A normalized score (100 indicating no symptoms and 0 indicating extreme symptoms) is calculated by adding the subscales together.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age of eighteen or older

  • Diagnosis of symptomatic knee osteoarthritis

  • Radiographic evidence of knee osteoarthritis

  • Failure of conservative treatment

Exclusion Criteria:
  • Treatment with any intra-articular knee injection within 8 weeks before surgery

  • Any disease or condition potential to interfere study outcome

  • Under 18 years of age

Contacts and Locations

Locations

Site City State Country Postal Code
1 Second affiliated hospital, school of medicine, Zhejiang Uni. Hangzhou Zhejiang China 310058

Sponsors and Collaborators

  • Second Affiliated Hospital, School of Medicine, Zhejiang University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Second Affiliated Hospital, School of Medicine, Zhejiang University
ClinicalTrials.gov Identifier:
NCT03788265
Other Study ID Numbers:
  • lipo-knee OA-dxs
First Posted:
Dec 27, 2018
Last Update Posted:
Apr 16, 2019
Last Verified:
Apr 1, 2019
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 16, 2019