Clinical Trials/ChiCTR2000035712

ChiCTR2000035712Active, not recruitingEarly Phase 1

眼内压升高后眼内结构及房水流畅系数变化的观察性研究

自费1 site in 1 country30 target enrollmentStarted: August 15, 2020Last updated: August 23, 2020

Trial Snapshot

Phase: Early Phase 1
Status: Active, not recruiting
Sponsor
Enrollment: 30
Locations: 1
Primary Endpoint: 眼压

Study Overview Study Design Eligibility Criteria Arms & Interventions Outcomes Investigators Sites Records & Identifiers Similar Trials

Study Overview

Brief Summary

本研究的目的是探讨眼压、传统房水流出通道结构和房水流畅系数之间的关系。

Study Design

Study Type: 观察性研究
Primary Purpose: 连续入组
Masking: N/a

Eligibility Criteria

Ages: 18 to 30 (—)
Sex: All

Inclusion Criteria

•（1）眼压<21mmhg，眼底镜检查视神经正常（双眼杯盘比<0.5，双眼杯盘比相差<0.2，无出血及边缘局限性或弥漫性变薄）；
•（3）入组前一个月内无影响循环系统的用药史。

Exclusion Criteria

•（1）最佳矫正视力<20/20；
•（2）屈光不正（RE）≤-6.0D 和 RE≥+3.0D；
•（3）存在其他眼部疾病，如年龄相关性黄斑变性、视网膜脱离或眼科手术史；
•（4）患有高血压或糖尿病，或者有这些疾病的家族史。

Arms & Interventions

case series

Outcomes

Primary Outcomes

眼压

Time Frame: 顶压眼球后 1min、2min、3min、4min 时

前段 OCT

Time Frame: 顶压前、顶压后即时、顶压后 1min、2min、3min、4min

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor

自费

Study Sites (1)

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