JPRN-jRCTa050200122进行中(未招募)1 期
allogeneic iPS cell-derived retinal pigmented epithelium (RPE) cell suspension for RPE impaired disease - aiPSC-RPE CS transplantation forRID
Kurimoto Yasuo0 个研究点目标入组 50 人开始时间: 2021年1月28日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 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) male or female at 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
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