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临床试验/NCT03110679
NCT03110679已完成4 期

Randomized Double-blind Study on the Treatment of Osteoarthritis of the Bilateral Knee: Autologous Bone Marrow Concentrate vs. Hyaluronic Acid

Istituto Ortopedico Rizzoli2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年5月23日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
60
试验地点
2
主要终点
International Knee Documentation Committee (IKDC)-Subjective score

研究概览

简要总结

OA-bi-Blind is a randomized double-blind study on the treatment of osteoarthritis of the Bilateral knee: autologous bone marrow concentrate vs. hyaluronic acid.

详细描述

a randomized, controlled, double-blind study and we will be evaluated and compared the clinical and radiological results of concentrated autologous bone marrow against the hyaluronic acid in patients with bilateral knee osteoarthrosis . In randomization, one knee will be treated with autologous bone marrow concentrate and other knee with hyaluronic acid, then every patient is considered both in control and treatment group, limiting the heterogenity between groups and will not be informed of the knee assigned to the treatment group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

cover the syringe to mask the contents

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients, aged between 18 and 75 years;
  • Bilateral symptomatic knee osteoarthritis (Kellgren-Lawrence grade 1-4);
  • Failure after two months of conservative treatment;
  • Capacity and consent of patients to participate actively in the rehabilitation protocol, follow-up clinic and radiology protocol;
  • Signature of informed consent.

排除标准

  • Patients incapable of discernment;
  • Patients with malignancy
  • Patients with rheumatic diseases;
  • Patients with diabetes;
  • Patients with metabolic disorders of the thyroid;
  • Patients belonging abuse of alcohol, drugs or medications;
  • Patients with misalignment of the lower limbs than 10 °;
  • Body Mass Index> 40;
  • Patients with a history of trauma or intra-articular infiltration of therapeutic substances within 6 months prior to treatment.

结局指标

主要结局

International Knee Documentation Committee (IKDC)-Subjective score

时间窗: Time Frame: 6 months

Clinical improvement, measured by the change in scores IKDC Subjective

次要结局

  • International Knee Documentation Committee (IKDC)-Subjective score(Time Frame: 1,3,6, 12, 24 months evaluation)
  • Knee Injury and Osteoarthritis Outcome Score (KOOS).(Time Frame: 1,3,6, 12, 24 months evaluation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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