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Completed

NCT Number: NCT01453738

Allogeneic Mesenchymal Stem Cells in Osteoarthritis

This trial is planed to study if allogeneic mesenchymal stem cells would be safe and beneficial in osteoarthritis of knee joint. This is a double blind study. Different doses of stem cells will be used in this study.

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Key information

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of Orthopedics, M. S. Ramaiah Memorial Hospital, Bangalore, Karnataka, India

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males or females in the age 40 - 70 years (both inclusive)
  • Radiographic evidence of grade 2 to 3 osteoarthritis based on the Kellgren and Lawrence radiographic criteria.
  • History of primary idiopathic osteoarthritis of the knee characterized by pain which requires intake of analgesics.
  • Self-reported difficulty in at least one of the following activities attributed to knee pain: lifting and carrying groceries, walking 400 metres, getting in and out of a chair, or going up and down stairs.
  • Patients who have been on stable medication which may be NSAIDs / Opioid or opiate analgesics, for the past three months.
  • Female patients of childbearing age must be willing to use accepted methods of contraception during the course of the study
  • Ability to provide written informed consent.

Exclusion criteria

  • Prior or ongoing medical conditions (e.g., concomitant illness, psychiatric condition, alcoholism, drug abuse), medical history, physical findings, ECG findings, or laboratory abnormality that, in the investigator's opinion, could adversely affect the safety of the subject, makes it unlikely that the course of treatment or follow-up would be completed, or could impair the assessment of study results.
  • History of surgery, or major trauma to the study joint
  • Arthroscopy on the study joint in the previous 12 months
  • Signs of active study joint inflammation including redness, warmth, and/or, if qualifying with osteoarthritis of the knee, a large, bulging effusion of the study knee joint with the loss of normal contour of the joint at the screening visit or at the baseline examination
  • Patients who had received intraarticular steroids or hyaluronan within the last three months.
  • Infections in or around the knee.
  • Patients awaiting a replacement knee or hip joint
  • Patients with other conditions that cause pain
  • Patients with deformity of the knee joint.
  • Significantly incapacitated or disabled and would be categorized as ACR Functional Class IV (largely or wholly incapacitated), or unable to walk without assistive devices
  • Patients with other known rheumatic or inflammatory disease such as rheumatoid arthritis
  • Other pathologic lesions on x-rays of knee
  • Positive hepatitis B surface antigen, hepatitis C antibody test, Anti human immunodeficiency virus (HIV) antibody test, or RPR
  • History of Bleeding disorders
  • Known hypersensitivity to Hyaluronan products or animal sera
  • For women of child-bearing potential: positive pregnancy test or lactating [Females who are planning pregnancy within next one year should be excluded]

Treatment and study plan

Ex- vivo cultured adult allogeneic MSCs

Biological

Single intraarticular dose of allogeneic MSCs suspended in 2ml Plasmalyte followed by 2ml of Hyaluronan

Plasmalyte-A

Biological

Single intraarticular dose of 2ml Plasmalyte followed by 2ml Hyaluronan

Primary outcomes

  1. Number and percentage of patients with adverse events as a measure of safety and tolerability

    Time frame: 2 years

    • Safety evaluation will include assessment of physical examination, periodic monitoring of vital signs (heart rate, respiratory rate, blood pressure and temperature), clinical laboratory investigations (including haematology, serum chemistry, LFT, urine-analysis) and 12-lead ECG recording.
    • Tolerability: Adverse events monitored using information volunteered by the patients and as observed by the PI will be summarized descriptively by total number of AE(s) and compared between the study arms.

Secondary outcomes

  1. Change from baseline in the WOMAC OA (Western Ontario and McMaster Universities Osteoarthritis) Index -pain subscale score

    Time frame: 2 years

  2. Change from baseline in WOMAC OA stiffness index

    Time frame: 2 years

  3. Change from baseline in WOMAC OA composite index

    Time frame: 2 years

  4. Change from baseline in ICOAP (Intermittent and Constant Osteoarthritis Pain)

    Time frame: 2 years

  5. Change from baseline in radiographic (X-ray) findings of knee

    Time frame: 2 years

  6. Change from baseline in the WORMS score (Whole-Organ Magnetic Resonance Imaging Score) of knee using MRI

    Time frame: 2 years

  7. Change from baseline in arthritis pain scores on the visual analogue scale

    Time frame: 2 years

  8. Reduction in the intake of analgesic tablets from baseline

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Stempeutics Research Pvt Ltd

Industry

Registry information

Official study title

A Randomized, Double Blind, Multicentric, Placebo Controlled, Phase -II Study Assessing the Safety and Efficacy of Intraarticular Ex-vivo Cultured Adult Allogeneic Mesenchymal Stem Cells in Patients With Osteoarthritis of Knee

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Oct 18, 2011
Registry last updated
May 12, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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