- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01446367
Corneal Changes After Retinal Surgery
October 4, 2011 updated by: Alexandre Grandinetti, Universidade Federal do Paraná
Corneal Topographic Changes After 20-gauge Pars Plana Vitrectomy Associated With Scleral Buckling for the Treatment of Rhegmatogenous Retinal Detachment
The purpose of this study is to evaluate the corneal changes after performing 20 gauge vitrectomy associated with scleral buckling for the treatment of rhegmatogenous retinal detachment.
Study Overview
Status
Completed
Conditions
Detailed Description
Patients submitted to 20-gauge vitrectomy associated with scleral buckling were evaluated with corneal topography before surgery and in the 7,30 and 90 days after surgery to asses corneal curvature changes.
Study Type
Observational
Enrollment (Actual)
25
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with rhegmatogenous retinal detachments
Description
Inclusion Criteria:
- Patients with rhegmatogenous retinal detachments
Exclusion Criteria:
- Previous eye surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2010
Primary Completion (Actual)
February 1, 2011
Study Completion (Actual)
February 1, 2011
Study Registration Dates
First Submitted
October 3, 2011
First Submitted That Met QC Criteria
October 4, 2011
First Posted (Estimate)
October 5, 2011
Study Record Updates
Last Update Posted (Estimate)
October 5, 2011
Last Update Submitted That Met QC Criteria
October 4, 2011
Last Verified
October 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cornea vs Vit-buckle
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.
Clinical Trials on Rhegmatogenous Retinal Detachment
-
University College, LondonNot yet recruitingProliferative Vitreoretinopathy | Retinal Detachment Rhegmatogenous | Proliferative Vitreoretinopathy in Rhegmatogenous Retinal DetachmentUnited Kingdom
-
Minia UniversityRecruitingRhegmatogenous Retinal DetachmentEgypt
-
Eye & ENT Hospital of Fudan UniversityRecruiting
-
Eye & ENT Hospital of Fudan UniversityNot yet recruitingRhegmatogenous Retinal DetachmentChina
-
Ain Shams UniversityNot yet recruitingRhegmatogenous Retinal Detachment
-
Sohag UniversityRecruiting
-
The S.N. Fyodorov Eye Microsurgery State InstitutionUnknownRhegmatogenous Retinal DetachmentRussian Federation
-
Meir Medical CenterUnknownRhegmatogenous Retinal DetachmentIsrael
-
University of Campinas, BrazilCompletedRhegmatogenous Retinal Detachment
-
WardahCompletedVitrectomy | Retina Disorder | Retinal Detachment RhegmatogenousPakistan