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临床试验/JPRN-jRCTa050210178
JPRN-jRCTa050210178招募中1 期

allogeneic iPS cell-derived retinal pigmented epithelium (RPE) cell strip for RPE impaired disease - aiPSC-RPE CSt transplantation forRID )

Kurimoto Yasuo0 个研究点目标入组 50 人开始时间: 2022年2月22日最近更新:
适应症

试验速览

阶段
1 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 ot applicable(—)
性别
All

入选标准

  • 1) clinically diagnosed as RPE impaired disease on the diagnostic criteria
  • 2) 20 years of age or older
  • 3) Window defect is observed by FAG.
  • 4) collected visual acuity is less than 0.3 or less, or visual field measured with Goldman dynamic quantitative visual field (target: V-4) is within 20 degrees, or Estherman static quantitative visual field is 70 points or less.
  • 5) Capable of understanding the documents of the research context and of informed consent and is able to provide a written informed consent

排除标准

  • 1) Ocular infection
  • 2) Glaucoma with poorly controlled intraocular pressure
  • 3) The affected eye was received intraocular surgeries other than cataract surgery within 3 months
  • 4) Any of bilirubin level, albumin level, and prothrombin time is outside the normal range as a criterion for liver function.
  • 5) Either creatinine level or eGFR (estimated glomerular filtration rate) is outside the normal range as a standard for renal function.
  • 6) B hepatitis virus, C hepatitis virus, human immunodeficiency virus, adult T-cell leukemia virus, cases of syphilis-positive
  • 7) Unable to quit anti-coagulants or antiplatelet medication
  • 8) Malignant carcinoma or its history in the past 3 years, however, this does not exclude patients with a history of carcinoma in situ.
  • 9) Family history of hereditary tumors
  • 10) Patients with contraindications for contrast agents, such as fluorescein or indocyanine green, antibacterial agents, steroids, immunosuppressants or anesthetics used in this clinical study
  • 11) May be pregnant during lactation or lactation. The patient or partner is planning a pregnancy.
  • 12) Participating in clinical studies involving other clinical trials or interventions within 1 month before obtaining consent or at the present time.
  • 13) Judged inadequate by the principal investigator and coresearchers
  • 14) When the case review meeting determines that it is unsuitable.

研究者

发起方
Kurimoto Yasuo

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