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Autologous Bone Marrow Aspirate Concentrate Injection for the Treatment of Early Osteoarthritis:Baghdad 2022

Primary Purpose

Treatment Complication

Status
Recruiting
Phase
Not Applicable
Locations
Iraq
Study Type
Interventional
Intervention
autologous bone marrow aspirate concentrate by centrifugation
Sponsored by
Global Stem Cell Center, Baghdad
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Treatment Complication

Eligibility Criteria

55 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Radiological diagnosis of Osteoarthritis according to Kellgren and Lawrence Criteria stage II-III.

    • Radiological grading of osteoarthritis of the knee determined by qualified radiologist using MOAKS scoring system.
    • Primary osteoarthritis not responsive to conventional treatment and physiotherapy.
    • A minimum pain score of 5 on an 11-point numerical scale.
    • Age >55 years

Exclusion Criteria:

  • Pregnancy and breast feeding.
  • Knee symptom due to other condition like tumor or referred pain from lumbar spine.
  • MRI confirmed displaced meniscal tear
  • MRI confirmed Grade IV chondral loss.
  • Previous knee surgery within the last 12 months.
  • Previous intra-articular injectable therapies within the last 6 months
  • History of severe systemic illness.
  • Active neoplasm under treatment in the last 12 months- Health conditions including known allergy to local
  • Bleeding tendency.

Sites / Locations

  • Ministry of HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

treatment with autologous bone marrow aspirate concentrate

control

Arm Description

autologous bone marrow aspirate is taken under local anesthesia to be centrifuged and the concentrate given intra articularly in knee joint

control group given analgesics only

Outcomes

Primary Outcome Measures

clinical
improvement in pain scale WOMAC

Secondary Outcome Measures

radiological proof
MRI of the knee joint to monitor effect

Full Information

First Posted
December 24, 2021
Last Updated
September 27, 2023
Sponsor
Global Stem Cell Center, Baghdad
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1. Study Identification

Unique Protocol Identification Number
NCT05193877
Brief Title
Autologous Bone Marrow Aspirate Concentrate Injection for the Treatment of Early Osteoarthritis:Baghdad 2022
Official Title
Autologous Bone Marrow Aspirate Concentrate Injection for the Treatment of Early Osteoarthritis: a Randomized Controlled Trial, Ibn-Sina Hospital, Baghdad 2022
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 8, 2022 (Actual)
Primary Completion Date
December 24, 2023 (Anticipated)
Study Completion Date
December 24, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Global Stem Cell Center, Baghdad

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
We present a randomized controlled trial (RCT) to assess the efficacy of autologous bone marrow aspirate concentrate BMAC of 1.8x 10 9 median cellular content in the treatment of early symptomatic knee OA. We use 2 injections 2 months apart (8).
Detailed Description
To evaluate the efficacy of bone marrow aspirate concentrate (BMAC) therapy on pain, function and disease modification in knee osteoarthritis. To determine the potential of BMAC therapy to achieve disease modification, as detected through radiological examination using magnetic resonance imaging (MRI) techniques. Methodology: A randomized controlled trial will be held in Ibn-Sina training hospital in Baghdad. All participants will complete written informed consent. The study will be a single centered trial. The trial design will consist of 60 participant randomly and equally allocated to control and treatment group by simple random sampling. Participants will not be blinded to their treatment allocation. Control group will receive conventional treatment only. Intervention group will receive (2 injections) intra-articular injections of (4cc) per joint at (8 weeks' interval). Intervention: 50 cc bone marrow aspirates concentrate after centrifugation with final volume up to 7 cc. Assess total nucleated count and viability. Bone marrow aspirate concentrate is chosen as a source of mesenchymal stem cells, because of safe and easy procedure. Bone marrow aspiration is done under local or general anesthesia, depending on the individual case. Around 50 cc of bone marrow is aspirated from the posterior iliac crest after proper sterilization using bone marrow aspiration needle (size according to the patient) and collected in heparinized syringes. Mononuclear cells (MNCs) are obtained by centrifugation. The isolated MNCs are checked for viability manually and confirmed on automated cell count machine. The separated MNCs is administered intra-articularly immediately after centrifugation. Place: Bone marrow aspiration and centrifugation procedure is done in clean area, in operation room HEPA filtered with all instruments included. Cell count viability and flow cytometry can be sent to nearby lab.CD markers (90, 44,29,105,34). Instruments: Bone marrow aspiration kit, centrifuge, automated cell counter. Sample size and sampling technique: The conventional treatment is usually classic treatment . Statistical analysis: Raw data will be summarized, and presented in appropriate table. The statistical analysis will be carried out using SPSS (statistical package for social science) software version 25

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Treatment Complication

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
double blind
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
treatment with autologous bone marrow aspirate concentrate
Arm Type
Active Comparator
Arm Description
autologous bone marrow aspirate is taken under local anesthesia to be centrifuged and the concentrate given intra articularly in knee joint
Arm Title
control
Arm Type
Sham Comparator
Arm Description
control group given analgesics only
Intervention Type
Procedure
Intervention Name(s)
autologous bone marrow aspirate concentrate by centrifugation
Intervention Description
50 cc bone marrow aspirates concentrate after centrifugation with final volume up to 7 cc. Assess total nucleated count and viability. Bone marrow aspirate concentrate is chosen as a source of mesenchymal stem cells, because of safe and easy procedure. Bone marrow aspiration is done under local or general anesthesia, depending on the individual case. Around 50 cc of bone marrow is aspirated from the posterior iliac crest after proper sterilization using bone marrow aspiration needle (size according to the patient) and collected in heparinized syringes. Mononuclear cells (MNCs) are obtained by centrifugation. The isolated MNCs are checked for viability manually and confirmed on automated cell count machine. The separated MNCs is administered intra-articularly immediately after centrifugation.
Primary Outcome Measure Information:
Title
clinical
Description
improvement in pain scale WOMAC
Time Frame
6 months
Secondary Outcome Measure Information:
Title
radiological proof
Description
MRI of the knee joint to monitor effect
Time Frame
6 months-1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Radiological diagnosis of Osteoarthritis according to Kellgren and Lawrence Criteria stage II-III. Radiological grading of osteoarthritis of the knee determined by qualified radiologist using MOAKS scoring system. Primary osteoarthritis not responsive to conventional treatment and physiotherapy. A minimum pain score of 5 on an 11-point numerical scale. Age >55 years Exclusion Criteria: Pregnancy and breast feeding. Knee symptom due to other condition like tumor or referred pain from lumbar spine. MRI confirmed displaced meniscal tear MRI confirmed Grade IV chondral loss. Previous knee surgery within the last 12 months. Previous intra-articular injectable therapies within the last 6 months History of severe systemic illness. Active neoplasm under treatment in the last 12 months- Health conditions including known allergy to local Bleeding tendency.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
abdulmajeed hammadi, MD
Phone
+9647902268105
Email
majeed51578@yahoo.co.uk
Facility Information:
Facility Name
Ministry of Health
City
Baghdad
ZIP/Postal Code
964
Country
Iraq
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
abdulmajeed A Hammadi, MD
Phone
+9647902268105
Email
adnanmj@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Autologous Bone Marrow Aspirate Concentrate Injection for the Treatment of Early Osteoarthritis:Baghdad 2022

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