MedPath

Study of retinal venous pressure measured by Contact Lens Dynamometer

Not Applicable
Conditions
vitreoretinal disease
Registration Number
JPRN-UMIN000025106
Lead Sponsor
Osaka Medical College
Brief Summary

Comparison of the BRVOs and CRVOs showed that VA was significantly improved by a single injection in BRVOs (P < 0.0001; P = 0.1087 for CRVOs), but CRT and RVP were significantly decreased without significant difference in IOP after the treatment in both groups (P < 0.0001).

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
26
Inclusion Criteria

Not provided

Exclusion Criteria

patients who is difficult to be measured retinal venous pressure.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
blood test and measurement of retinal venous pressure before and 1 month, 6 months after the treatment.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath