Search for Biomarkers in Human Glaucoma: Lymphocytes Alterations and Rate of Progression
NCT ID: NCT00981422
Last Updated: 2009-09-22
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
40 participants
OBSERVATIONAL
2007-06-30
2008-06-30
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.
mRNA Expression in Lymphocytes of Glaucoma Patients
NCT00327509
Autoimmune Dysregulation in Pigmentary Glaucoma
NCT00280345
Evaluation of Rate of Progression With Perimetry in Newly Diagnosed Open Angle Glaucoma
NCT02379208
Advanced Glaucoma Progression Study
NCT01742819
Central Corneal Thickness in Glaucoma
NCT01023997
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_CONTROL
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Glaucoma patients
POAG patients selected by an ophthalmologist from the Glaucoma Service, Ophthalmology Institute, University of Parma
No interventions assigned to this group
Healthy
healthy subjects with negative history for (a) neurodegenerative diseases, (b) autoimmune diseases, (c) cancer, (d) viral infection, (e) diabetes, and (f) systemic inflammation
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age between 19 an 85 years old
Exclusion Criteria
* positive history for (a) neurodegenerative diseases, (b) autoimmune diseases, (c) cancer, (d) viral infection and (e) diabetes, (f)systemic inflammation
19 Years
85 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Parma
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
UNIVERSITY OF PARMA
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Stefano A Gandolfi, MD
Role: PRINCIPAL_INVESTIGATOR
Ophthalmology Institute, University of Parma, Italy
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Azienda ospedaliera universitaria
Parma, , Italy
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.
PARMABIOMARKERS001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.