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临床试验/JPRN-jRCTs042190030
JPRN-jRCTs042190030招募中1 期

The surgical repair of refractory ocular surface diseases using Hyper dry human amniotic membrane (HD-AM);including patients that are out of advanced medical careB(Surgical reconstruction using the hyper dry human amniotic membrane : recurrence pteryg ium (proliferative tissue is limited to a thing more than the limbus.)) - SROHD-AM

Hayashi Atsushi0 个研究点目标入组 52 人开始时间: 2019年5月27日最近更新:

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
52

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)1:Pterygium/including Scleral malacia/Conjunctival tumor(Intraconjunctival hyperplasia), 2:Corneal perforation/Conjunctival perforation, 3:Glaucoma bleb leak/Glaucoma bleb scarring, 4:Corneal/conjunctival epithelial defect (including Corneal scar, induced by the Corneal transplantation), 5:Symblepharon adhesion (including Stevens-Johnson Syndrome, Pemphigoid of the eye, Thermochemical trauma scar, heavy Scarring keratoconjunctival disease)
  • 2) more than 20 years-old
  • 3)The patients with relatively good general condition
  • 4) The patients whom it is judged to be available for observation, the testing that conformed to a study enforcement plan and a survey.

排除标准

  • 1)The patients whom a doctor judg ed safely for study period if it was difficult hospital visiting and to come home.
  • 2)The patients who complicate eye infection with activity.
  • 3)The patients who plan the enforcement of eye operations for evaluation eyes effective during study period in (we assume the ag reement acquisition study initiation).
  • 4)one eyes are the patients of enucleation eyes or evisceration eyes.
  • 5)For the g roup medicine of the planned drug(dropping lotion in the eyes anesthetic ag ent, fluorescein) to use during study period, it is the patients with a history of the drug allergy.
  • 6)The patients (saying that, however, the subjects who do not receive the study drug are possible) who participated in other studies or clinical studies within six months.
  • 7) Preg nancy or the childbearing patients who may be preg nant or hope for preg nancy during study period or do not use appropriate contraception.
  • 8) Patients who can be entried Advanced Medical B (jRCTs 042180103).
  • 9)The patients who were judg ed to be inadequate as an object of this study in testing at agreement acquisition by doctor.

研究者

发起方
Hayashi Atsushi

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