- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01247155
First Postoperative Day Review After Uneventful Phacoemulsification
Study Overview
Status
Conditions
Study Type
Contacts and Locations
Study Locations
-
-
Imathia
-
Veroia, Imathia, Greece, 59100
- General Hospital of Veroia
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Exclusion Criteria:
Exclusion criteria were the following:
i) intra-operative complications, such as posterior capsule rupture, vitreous loss, lost nucleus, zonule dehiscence and wound leak,
ii) inadequate social support for overnight care at home,
iii) severely limited visual potential in the fellow eye,
iv) uveitis or ocular trauma,
v) severe systemic diseases limiting activity,
vi) patients with learning disability or dementia.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
first day review
|
non-first day review
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Best corrected visual acuity
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 9151
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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