Re-fixating Dislocated Scleral Fixing Intra-ocular Lens
NCT ID: NCT05278949
Last Updated: 2023-03-24
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
NA
5 participants
INTERVENTIONAL
2022-01-01
2023-03-21
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.
Sutureless Technique for Repositioning and Scleral Fixation of the Capsular Bag - Intraocular Lens Complex With Permanent Use of Iris Retractors
NCT07257172
Safety and Suitability of ICL for Correction of Refractive Errors Without the Use of Dispersive OVDs
NCT06371079
Clinical Outcomes of Implantationof Black Diaphragm Intraocular Lens in Complete Aniridia and Aphakia Due to Posttraumatic Eye Rupture
NCT03581864
Retinal Detachment After Lens Surgery in the Nearsighted
NCT04072939
Artisan Aphakia Lens for the Correction of Aphakia (Secondary) in Adults
NCT01547429
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Here, the investigators utilized the same participant's IOL with minimum manipulations and the haptic ends buried inside scleral pockets to prevent future exposure and complications. The pocket entry is sutured with 8/0 vicryl, which is absorbable, to overcome complications.
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.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
The scleral pocket for the primary implanted IOL
single arm
The surgical intervention
The participant's primary IOL is re-fixed without utilizing any new material.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
The surgical intervention
The participant's primary IOL is re-fixed without utilizing any new material.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Anterior chamber IOL
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Omer Othman Abdullah
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Omer Othman Abdullah
Associate consultant ophthalmologist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Omer Abdullah, M.Sc.
Role: PRINCIPAL_INVESTIGATOR
Ibinsina Modern Eye and Retina Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ibinsina Modern eye and retina center
Erbil, , Iraq
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.
IMER 14
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.