INMUNOCEM-OA: Cartilage Recovery in Adults With Knee Osteorthritis by Mesenchymal Cell Therapy: Randomized Trial of Radiologic and Clinical Outcomes

Sponsor
GUSTAVO SALGUERO (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05936060
Collaborator
Hospital Infantil Universitario de San Jose (Other)
32
2
34

Study Details

Study Description

Brief Summary

The treatment of osteoarthritis (OA) of the knee remains still controversial. Despite that fact advanced stages with symptomatic and functional improvement are obtained with total knee replacement, however, there is no treatment that neither modifies the natural history of this disease, nor avoid joint replacement surgery in young patients in whom the prosthesis has conflictive indications. Moreover, prosthetic surgery leads to lower long-term survival and in older patients, higher morbidity and mortality. Cell therapy promises to be a treatment option through the use of mesenchymal cells with the capacity control inflammatory responses and trigger the differentiation into chondrocytes. Here we propose a randomized placebo-controlled clinical trial to evaluate radiologic and clinical outcomes in patients with knee OA.

Condition or Disease Intervention/Treatment Phase
  • Biological: INMUNOCEM
  • Drug: PLACEBO COMPARATOR
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Recovery of Joint Cartilage in Adults With Knee Osteoarthritis by Use of Mesenchymal Stromal Cells Derived From Human Umbilical Cord: Randomized Controlled Clinal Trial With Clinical and Radiologic Outcomes
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Jul 31, 2026
Anticipated Study Completion Date :
Jul 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: IMUNOCEM

Administration of umbilical cord-derived mesenchymal stromal cells suspension

Biological: INMUNOCEM
Mesenchymal Stromal Cell suspension intraarticularly injected
Other Names:
  • Mesenchymal stromal cell suspension
  • Placebo Comparator: PLASMALYTE

    Administration of plasmalyte as vehicle for MSC

    Drug: PLACEBO COMPARATOR
    Administration of plasmalyte as a vehicle for MSC
    Other Names:
  • PLASMALYTE
  • Outcome Measures

    Primary Outcome Measures

    1. Changes in Visual Analogue scale (VAS) [30 months (day 0, day 1, month 1, month 3, month 6, year 1 and year 2]

      The pain VAS is a unidimensional measure of pain intensity, used to record patients' pain progression, or compare pain severity between paints with similar conditions. Score ranges from 1 to 10, where 1 means lowest pain and 10 relates to highest pain

    2. Changes in Knee Injury and Osteoarthritis Outcome Score (KOOS) [30 months (day 0, month 3, month 6, year 1 and year 2)]

      KOOS reflects the individual disease burden and overall joint health. 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). The previous week is the time period considered when answering the questions. A normalized score (100 indicating no symptoms and 0 indicating extreme symptoms) is calculated for each subscale

    3. Radiological changes in Magnetic resonance observation of cartilage repair tissue (MOCART 2.0) [30 Months (day 0, year 1 and year 2)]

      MOCART score was introduced based on 7 pertinent variables that facilitate a standardized, reproducible, semiquantitative approach for the morphological assessment of cartilage repair. Variables assesed in MOCART are: 1. Degree of cartilage defect; 2. integration into adjacent cartilage; 3. surface of the repair tissue; 4. structure of the repair tissue; 5. signal intensity of repaired tissue; 6. bony defect or bony overgrowth; 7. subchondral changes. The score ranges between 0 and 100, being 100 the maximum level of tissue compromise

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 60 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Pain most days for the last month. Presence of osteophytes. Synovial fluid with mechanical characteristics. Morning stiffness for less than 30 minutes in the affected joint. Patellar crepitus. Patients aged 40 years or older and less than 60 years. Radiological criteria for osteoarthritis of the knee Kellgren-Lawrence 2 to 4 in comparative radiographs with knee support taken in the last 12 months prior to consultation.

    Pain in one or both knees according to a visual analogue scale of 5 or more, out of 10 points in the last 3 months.

    Exclusion Criteria:

    Consumption of non-steroidal anti-inflammatory drugs or anticoagulants in the last 14 days.

    Patient with a history of joint infiltration or arthroscopic surgery of the affected knee in the last 6 months.

    Participants in another treatment or research study within the past year. Pregnant or lactating patients. Patient with active tumor pathology or a history of oncological disease. Patient with metabolic disease and/or uncontrolled coagulopathy at the assessment time.

    Patients who have received previous treatments such as microfractures, and osteochondral allografts.

    Patients with present meniscal lesions. Patients with a history of thyroiditis or thyroid nodules with increased antithyroglobulin antibodies.

    Patients with a history of osteoarticular infection in the last 5 years or active at the time of assessment.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • GUSTAVO SALGUERO
    • Hospital Infantil Universitario de San Jose

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    GUSTAVO SALGUERO, Research Leader Advanced Therapies Unit, Instituto Distrital de Ciencia, Biotecnología e Innovación en Salud - IDCBIS
    ClinicalTrials.gov Identifier:
    NCT05936060
    Other Study ID Numbers:
    • IDCBIS-UTA-EC-01-InmunoCEM
    First Posted:
    Jul 7, 2023
    Last Update Posted:
    Jul 7, 2023
    Last Verified:
    Jun 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 7, 2023