Comparison of Scheimpflug Photos of the Crystalline Lens in Patients Who Have Undergone Vitrectomy Surgery and Controls
NCT ID: NCT00406263
Last Updated: 2016-07-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
49 participants
OBSERVATIONAL
2006-11-30
2010-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Corneal Endothelial Cell Loss After Phacoemulsification Compared With Extracapsular Cataract Extraction
NCT03262285
NPI-002 Intravitreal Implant for the Delay of Cataract Progression
NCT05026632
Comparison of In-the-bag Stability Between Single-piece and Three-piece Intraocular Lens
NCT02609997
Assessment Of Anterior Chamber Configuration Changes After Phacoemulsification
NCT02238002
Correlation Analysis of Lens Nucleus Density and Surgical Parameters Based on Ss-oct and Scheimpflug Technology
NCT05028530
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Scheimpflug crystalline lens photographs
scheimpflug photographs
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* controls will be phakic eyes of patients that have not undergone andy kind of intraocular surgery,
* age 18 and older
Exclusion Criteria
* has had previous vitreoretinal surgery,
* has had previous intravitreal injection,
* previous intraocular inflammatory condition such as uveitis,
* previous irradiation,
* any patient with a history of ocular malignancy,
* history of infectious intraocular condition
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Barnes Retina Institute
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Rhonda Weeks
Nancy Holekamp, MD, Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nancy M Holekamp, MD
Role: PRINCIPAL_INVESTIGATOR
Barnes Retina Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Barnes Retina Institute
St Louis, Missouri, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
06-1016
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.