search
Back to results

Treatment of Osteoarthritis by Intra-articular Injection of Bone Marrow Mesenchymal Stem Cells With Platelet Rich Plasma (CMM-PRGF/ART)

Primary Purpose

Knee Osteoarthritis

Status
Unknown status
Phase
Phase 1
Locations
Spain
Study Type
Interventional
Intervention
100 million Bone marrow mesenchimal stem cells
Platelet Rich plasma (PRGF)
Sponsored by
Clinica Universidad de Navarra, Universidad de Navarra
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Knee Osteoarthritis focused on measuring Knee Osteoarthritis, Mesenchimal stem cell, Osteoarthritis

Eligibility Criteria

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

Inclusion Criteria:

  • Males and females between 40 and 80 year old
  • Bad results with previous hyaluronic acid injection
  • Diagnosis of knee OA according to the criteria of osteoarthritis of the ACR (American College of Rheumatology)
  • Joint pain equal or greater than 2.5 points on the visual analogue scale (VAS)
  • Radiological Classification: Kellgren-Lawrence scale greater or equal to 2
  • Body mass index between 20 and 35 kg/m2
  • Ability to follow during the study period

Exclusion Criteria:

  • Bilateral Osteoarthritis of the Knee requiring treatment in both knees
  • Previous diagnosis of polyarticular disease
  • Severe mechanical deformation
  • Arthroscopy during the previous 6 months
  • Intraarticular infiltration of hyaluronic acid in the last 6 months
  • Systemic autoimmune rheumatic disease
  • Poorly controlled diabetes mellitus
  • Blood dyscrasias
  • Immunosuppressive or anticoagulant treatments
  • Treatment with corticosteroids in the 3 months prior to inclusion in the study
  • NSAID therapy within 15 days prior to inclusion in the study
  • Patients with a history of allergy to penicillin or streptomycin

Sites / Locations

  • Hospital Universitario de Salamanca
  • Departamento Cirugía Ortopédica y Traumatología. Clinica Universidad de Navarra

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Platelet Rich Plasma (PRGF)

BMMSC with Platelet Rich Plasma (PRGF)

Arm Description

Platelet Rich plasma (PRGF) 3 intraarticular onjections sepataded by 7 days.

Single intraarticular injection of 100 million Bone marrow mesenchimal stem cells and three intraarticular injections of plateler Rich Plasma (PRGF) separatede by 7 days.

Outcomes

Primary Outcome Measures

Baseline Visual analogue scale (VAS) Baseline Visual analogue scale (VAS)
Baseline Visual analogue scale (VAS) prior to the initial dose on day 1
Baseline value of knee injury and osteoarthritis outcome score (Koos).
Prior to the intervention on day 1 value of knee injury and osteoarthritis outcome score (Koos).
Baseline Western Ontario and McMaster Universities Osteoarthritis Index score (WOMAC).
Universities Osteoarthritis Index score (WOMAC).
Baseline SF-36 value
Baseline SF-36 value
Baseline euroquol 5D value
Pretreatment euroquol 5D value
Baseline Lequesne index
Prior to the intervention on day 1 Lequesne index
Baseline femorotibial distance
Prior to the intervention femoritibial distance on rosenberg x-ray view
Number of Participants with Serious and Non-Serious Adverse Events Number of Participants with Serious and Non-Serious Adverse Events Number of Participants with Serious and Non-Serious Adverse Events
Participants with Serious and Non-Serious Adverse Events Number of Participants with Serious and Non-Serious Adverse Events During the follow up
Visual analogue scale (VAS) at 1 month
Visual analogue scale (VAS) at on month
Visual analogue scale (VAS) at 3 months
Visual analogue scale (VAS) at 3 months
Visual analogue scale (VAS) at 6 months
Visual analogue scale (VAS) at 6 months
Visual analogue scale (VAS) at 12 months
Visual analogue scale (VAS) at 12 months
Value of knee injury and osteoarthritis outcome score (Koos) at 1 month
Value of knee injury and osteoarthritis outcome score (Koos) at 1 month
Value of knee injury and osteoarthritis outcome score (Koos) at 3 month
Value of knee injury and osteoarthritis outcome score (Koos) at 3 month
Value of knee injury and osteoarthritis outcome score (Koos) at 6 month
Value of knee injury and osteoarthritis outcome score (Koos) at 6 month
Value of knee injury and osteoarthritis outcome score (Koos) at 12 months
Value of knee injury and osteoarthritis outcome score (Koos) at 12 months

Secondary Outcome Measures

Full Information

First Posted
July 18, 2014
Last Updated
October 23, 2017
Sponsor
Clinica Universidad de Navarra, Universidad de Navarra
search

1. Study Identification

Unique Protocol Identification Number
NCT02365142
Brief Title
Treatment of Osteoarthritis by Intra-articular Injection of Bone Marrow Mesenchymal Stem Cells With Platelet Rich Plasma
Acronym
CMM-PRGF/ART
Official Title
Phase I/II. Treatment of Osteoarthritis by Intra-articular Injection of Bone Marrow Mesenchymal Stem Cells With Platelet Rich Plasma(PRGF)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
June 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Clinica Universidad de Navarra, Universidad de Navarra

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Purpose: To determine the safety, feasibility and effectiveness (clinical and radiological) of intra-articular administration of autologous mesenchymal stem cells (MSCs) with platelet richa plasma (PRGF) in patients with knee osteoarthritis. Patients and methods Clinical trial phase I- II, randomized , multicenter , with two treatment arms and 19 patients for each group. The investigators compare the intraarticular injection of against the administration of two different doses of mesenchymal stem cells with hialuronic acid according to the following scheme: Group A: 3 intra-articular injections of platelet rich plasma (PRGF®) separated by 7 days. Group B: 3 intra-articular injections of platelet richa plasma (PRGF®) separated by 7 days and one with Mesenchimal stems cells. Intra-articular injection of 100 million autologous mesenchymal progenitor stem cells cultured ex - vivo (cell suspension sterile small volume (5-10 ml ) in a vehicle suitable for intraarticular injection ) followed by an intraarticular injection of platelet richa plasma (PRGF®). The treatment is completed with 2 more injection of platelet richa plasma (PRGF®) separeted by one week. In addition the investigators assess the response to intra-articular infusion of CMM analyzing the following parameters: Clinical assessment of pain and function (Baseline, 1, 3, 6 and 12 months since treatment): VAS , WOMAC , KOOS , EuroQol, SF-16, Lequesne , WOMAC , KOOS. Radiographic (baseline and 12 months from treatment): Femorotibial space. Radiographic using MRI (baseline and 12 months from treatment): by assessing the number location of the lesions , cartilage thickness , signal intensity , subchondral bone alteration , volume and WORMS and dGEMRIC protocols.
Detailed Description
Purpose: To determine the safety, feasibility and effectiveness (clinical and radiological) of intra-articular administration of autologous mesenchymal stem cells (MSCs) with platelet richa plasma (PRGF®) in patients with knee osteoarthritis. Patients and methods Clinical trial phase I- II, randomized , multicenter , with two treatment arms and 19 patients for each group. The investigators compare the intraarticular injection of against the administration of two different doses of mesenchymal stem cells with hialuronic acid according to the following scheme: Group A: 3 intra-articular injections of platelet richa plasma (PRGF®) separated by 7 days. Group B: 3 intra-articular injections of platelet richa plasma (PRGF®) separated by 7 days and one with Mesenchimal stem cell. Intra-articular injection of 100 million autologous mesenchymal progenitor stem cells cultured ex - vivo (cell suspension sterile small volume (5-10 ml ) in a vehicle suitable for intraarticular injection ) followed by an intraarticular injection of platelet richa plasma (PRGF®). The treatment is completed with 2 more injection of platelet richa plasma (PRGF®) separeted by one week. The autologous mesenchymal stem cells are obtained from the iliac crest under local anesthesia and sedation. They are cultured ex vivo The primary endpoint is safety and feasibility. The investigators registered the occurrence of complications and / or adverse effects during the study. In addition the investigators assess the response to intra-articular infusion of CMM analyzing the following parameters: Clinical assessment of pain and function (Baseline, 1, 3, 6 and 12 months since treatment): VAS , WOMAC , KOOS , EuroQol, SF-16, Lequesne , WOMAC , KOOS. Radiographic (baseline, 6 and 12 months since treatment): Femorotibial space. Radiographic using MRI (baseline, 6 and 12 months since treatment): by assessing the number location of the lesions , cartilage thickness , signal intensity , subchondral bone alteration , volume and WORMS and dGEMRIC protocols. All patients met the following inclusion and exclusion criteria:

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Knee Osteoarthritis, Mesenchimal stem cell, Osteoarthritis

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
38 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Platelet Rich Plasma (PRGF)
Arm Type
Active Comparator
Arm Description
Platelet Rich plasma (PRGF) 3 intraarticular onjections sepataded by 7 days.
Arm Title
BMMSC with Platelet Rich Plasma (PRGF)
Arm Type
Active Comparator
Arm Description
Single intraarticular injection of 100 million Bone marrow mesenchimal stem cells and three intraarticular injections of plateler Rich Plasma (PRGF) separatede by 7 days.
Intervention Type
Biological
Intervention Name(s)
100 million Bone marrow mesenchimal stem cells
Intervention Description
100 million Bone marrow mesenchimal stem cells with PRGF
Intervention Type
Biological
Intervention Name(s)
Platelet Rich plasma (PRGF)
Intervention Description
3 injections of PRGF
Primary Outcome Measure Information:
Title
Baseline Visual analogue scale (VAS) Baseline Visual analogue scale (VAS)
Description
Baseline Visual analogue scale (VAS) prior to the initial dose on day 1
Time Frame
Day 1
Title
Baseline value of knee injury and osteoarthritis outcome score (Koos).
Description
Prior to the intervention on day 1 value of knee injury and osteoarthritis outcome score (Koos).
Time Frame
Day 1
Title
Baseline Western Ontario and McMaster Universities Osteoarthritis Index score (WOMAC).
Description
Universities Osteoarthritis Index score (WOMAC).
Time Frame
Day 1
Title
Baseline SF-36 value
Description
Baseline SF-36 value
Time Frame
Day 1
Title
Baseline euroquol 5D value
Description
Pretreatment euroquol 5D value
Time Frame
Day 1
Title
Baseline Lequesne index
Description
Prior to the intervention on day 1 Lequesne index
Time Frame
Day 1
Title
Baseline femorotibial distance
Description
Prior to the intervention femoritibial distance on rosenberg x-ray view
Time Frame
Day 1
Title
Number of Participants with Serious and Non-Serious Adverse Events Number of Participants with Serious and Non-Serious Adverse Events Number of Participants with Serious and Non-Serious Adverse Events
Description
Participants with Serious and Non-Serious Adverse Events Number of Participants with Serious and Non-Serious Adverse Events During the follow up
Time Frame
Follow up (up to 12 months)
Title
Visual analogue scale (VAS) at 1 month
Description
Visual analogue scale (VAS) at on month
Time Frame
1 month
Title
Visual analogue scale (VAS) at 3 months
Description
Visual analogue scale (VAS) at 3 months
Time Frame
3 months
Title
Visual analogue scale (VAS) at 6 months
Description
Visual analogue scale (VAS) at 6 months
Time Frame
6 months
Title
Visual analogue scale (VAS) at 12 months
Description
Visual analogue scale (VAS) at 12 months
Time Frame
12 months
Title
Value of knee injury and osteoarthritis outcome score (Koos) at 1 month
Description
Value of knee injury and osteoarthritis outcome score (Koos) at 1 month
Time Frame
1 month
Title
Value of knee injury and osteoarthritis outcome score (Koos) at 3 month
Description
Value of knee injury and osteoarthritis outcome score (Koos) at 3 month
Time Frame
3 Months
Title
Value of knee injury and osteoarthritis outcome score (Koos) at 6 month
Description
Value of knee injury and osteoarthritis outcome score (Koos) at 6 month
Time Frame
6 months
Title
Value of knee injury and osteoarthritis outcome score (Koos) at 12 months
Description
Value of knee injury and osteoarthritis outcome score (Koos) at 12 months
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females between 40 and 80 year old Bad results with previous hyaluronic acid injection Diagnosis of knee OA according to the criteria of osteoarthritis of the ACR (American College of Rheumatology) Joint pain equal or greater than 2.5 points on the visual analogue scale (VAS) Radiological Classification: Kellgren-Lawrence scale greater or equal to 2 Body mass index between 20 and 35 kg/m2 Ability to follow during the study period Exclusion Criteria: Bilateral Osteoarthritis of the Knee requiring treatment in both knees Previous diagnosis of polyarticular disease Severe mechanical deformation Arthroscopy during the previous 6 months Intraarticular infiltration of hyaluronic acid in the last 6 months Systemic autoimmune rheumatic disease Poorly controlled diabetes mellitus Blood dyscrasias Immunosuppressive or anticoagulant treatments Treatment with corticosteroids in the 3 months prior to inclusion in the study NSAID therapy within 15 days prior to inclusion in the study Patients with a history of allergy to penicillin or streptomycin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
José Lamo-Espinosa, MD
Organizational Affiliation
Clinica Universidad de Navarra
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Felipe Prosper, MD, PhD
Organizational Affiliation
Clínica Universidad de Navarra
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Juan Blanco, MD; PhD
Organizational Affiliation
Complejo Universitario de Salamanca
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario de Salamanca
City
Salamanca
State/Province
Castilla-León
ZIP/Postal Code
37007
Country
Spain
Facility Name
Departamento Cirugía Ortopédica y Traumatología. Clinica Universidad de Navarra
City
Pamplona
State/Province
Navarra
ZIP/Postal Code
31008
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
32948200
Citation
Lamo-Espinosa JM, Blanco JF, Sanchez M, Moreno V, Granero-Molto F, Sanchez-Guijo F, Crespo-Cullel I, Mora G, San Vicente DD, Pompei-Fernandez O, Aquerreta JD, Nunez-Cordoba JM, Vitoria Sola M, Valenti-Azcarate A, Andreu EJ, Del Consuelo Del Canizo M, Valenti-Nin JR, Prosper F. Phase II multicenter randomized controlled clinical trial on the efficacy of intra-articular injection of autologous bone marrow mesenchymal stem cells with platelet rich plasma for the treatment of knee osteoarthritis. J Transl Med. 2020 Sep 18;18(1):356. doi: 10.1186/s12967-020-02530-6.
Results Reference
derived
Links:
URL
http://www.cun.es/actualidad/noticias/celulas-madre-osea-artrosis-rodilla
Description
University clinic of navarre trial information

Learn more about this trial

Treatment of Osteoarthritis by Intra-articular Injection of Bone Marrow Mesenchymal Stem Cells With Platelet Rich Plasma

We'll reach out to this number within 24 hrs