跳至主要内容
临床试验/NCT03698045
NCT03698045撤回1 期

Study to Evaluate the Safety and Tolerability of Pro-143 Ophthalmic Solution in Healthy Volunteers.

Laboratorios Sophia S.A de C.V.1 个研究点 分布在 1 个国家开始时间: 2013年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
试验地点
1
主要终点
Conjunctival bulbar hyperemia

研究概览

简要总结

Study to evaluate the safety and tolerability of PRO-143 solution ophthalmic in healthy volunteers.

详细描述

A phase I, open label and unicentric clinical trial to evaluate the safety and tolerability of PRO-143 ophthalmic solution in healthy volunteers.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Healthy male and female.
  • Age ≥ 18 years old at screening visit.

排除标准

  • Any ocular or systemic condition.
  • Patient with one blind eye.
  • Visual acuity of 20/40 in any eye.
  • Use of ocular or systemics medications.
  • Contraindications or sensitivity to any component of the study treatments.
  • Contact lens users.
  • Ocular surgery within the past 3 months..
  • Women who were not using an effective means of contraception or who were pregnant or nursing.
  • Participation in any studies of investigational drugs within 90 days previous to the inclusion.

研究组 & 干预措施

PRO-143 Ophthalmic Solution

Experimental

PRO-143 Ophthalmic Solution applied four times per day (c/6 hours) during 10 days.

干预措施: PRO-143 Ophthalmic Solution (Drug)

结局指标

主要结局

Conjunctival bulbar hyperemia

时间窗: 10 days

Conjunctival hyperemia is defined as the simplest reaction of the conjunctiva to a stimulus, a red appearance secondary to the vasodilation of the conjunctival vessels of variable intensity. He will graduate using the Efron scale. 0 Normal , 1 Very slight, 2 Mild, 3 Moderate, 4 Severe.

Number of Participants with adverse events

时间窗: 10 days

he evaluation of adverse events requires a questioning conducted by the principal investigator and the appropriate exploratory techniques for its detection. the number of adverse events per study group will be considered for the analysis

次要结局

  • Intraocular pressure (IOP)(10 days)
  • Visual ability (VA)(10 days)
  • Eye comfort index (ICO)(10 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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