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临床试验/JPRN-jRCT1080225305
JPRN-jRCT1080225305招募中2 期

Phase II Exploratory Study of EVA-001 for Osteoarthritis of the Knee

EVASTEM Co., Ltd.0 个研究点目标入组 50 人开始时间: 2020年8月7日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 80age old(—)
性别
All

入选标准

  • •1)Men and women between the ages of 20 and 80 years
  • •2)Patients with ICRS Grade 3 or 4 cartilage damage or deficiency in the knee joint as determined by magnetic resonance imaging (MRI) during the screening phase or by examination within the past 3 months.
  • •3)Patients with a K and L Grade of 2 to 4 based on simple x-ray examination
  • •4)Patients with an area of lesion damage of 2-9 cm2 that is the primary source of clinical symptoms
  • •5)Patients with knee flexion contractures of 10 degrees or less
  • •6)Patients who are eligible for high tibial osteotomy with a femoro-tibial angle (FTA) of 180 to 185 degrees.
  • •7)Patients with pain of 40 mm or more on the 100 mm VAS Scale
  • •8)Patients with a BMI of 35 kg/m2 or less
  • •9)Patients who do not wish to become pregnant during the trial period
  • •10)Patients who have voluntarily decided to participate in the trial and have signed the consent form.

排除标准

  • •Patients who meet any of the following criteria shall be excluded
  • •1)no remaining lateral cartilage due to progressive osteoarthritis of the knee
  • •2)autoimmune diseases or a history of such diseases
  • •3)an infection or suspected infection requiring parenteral antibiotics
  • •4)serious cardiovascular disease (myocardial infarction, congestive heart failure, uncontrolled hypertension, or other serious cardiac disease) or a history of such disease
  • •5)gout or suspected gout
  • •6)blood clotting abnormalities
  • •7)serious renal function abnormalities
  • •8)serious liver damage
  • •9)serious medical conditions
  • •10)malignancy or suspected malignancy
  • •11)who are pregnant or potentially pregnant
  • •12)who are currently breastfeeding
  • •13)mental disorders or a history of mental disorders
  • •14)who are habitual drinkers and are dependent or suspected of being alcoholic
  • •15)a mean number of cigarettes smoked per day x number of years of smoking to date of 200 or more, and patients who are nicotine dependent or suspected to be so.
  • •16)chronic inflammatory joint diseases (e.g., rheumatoid arthritis).
  • •17)who have received immunosuppressive drugs such as cyclosporine A or azathioprine within the past 6 weeks
  • •18)ligament fiber damage of Grade II or greater.
  • •19)paralysis due to nerve or muscle disease on the side of the knee joint cartilage damage or defect (affected side of the leg)
  • •20)a history of serious hypersensitivity to bovine-derived or porcine derived ingredients of this product
  • •21)a history of severe hypersensitivity or anaphylactic shock to gentamicin
  • •22)a history of severe hypersensitivity or anaphylactic shock to metal allergy
  • •23)a history of severe hypersensitivity or anaphylaxis to sodium hyaluronate or products containing hyaluronic acid.
  • •24)a history of blood transfusion or transplantation
  • •25)who have participated in another clinical trial within the past 3 months
  • •26)who have been at rest for a long period of time within the past 3 months
  • •27) with a history of contraindications to magnetic resonance imaging (MRI) or contrast media
  • •28) with meniscus locking symptoms
  • •29) Other patients who are determined to be unsuitable by the investigator or sub-investigator

研究者

发起方
EVASTEM Co., Ltd.

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