Actively Recruiting
Analysis of Risk Factors for High Intraocular Pressure and Retinal Detachment Recurrence After Vitrectomy with Silicone Oil Tamponade in Retinal Detachment Patients
Led by First Affiliated Hospital of Chongqing Medical University · Updated on 2025-02-14
65
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is a retrospective study. Patients who visited the ophthalmology clinic of the First Affiliated Hospital of Chongqing Medical University between September 1, 2024, and December 31, 2025, will be screened according to the inclusion and exclusion criteria mentioned below. After obtaining informed consent, clinical data of the subjects will be collected. The surgical procedure will involve "vitrectomy + retinal laser photocoagulation + retinal reattachment + silicone oil tamponade (+ cataract extraction + intraocular lens implantation)." Observation indicators will be recorded at various time points postoperatively: 1 day, 1 week, 1 month, 3 months, 6 months, and before silicone oil removal. Any emergent events occurring during the trial will be treated accordingly. Finally, data will be statistically analyzed to identify risk factors for high intraocular pressure and retinal detachment recurrence in patients with rhegmatogenous retinal detachment.
CONDITIONS
Official Title
Analysis of Risk Factors for High Intraocular Pressure and Retinal Detachment Recurrence After Vitrectomy with Silicone Oil Tamponade in Retinal Detachment Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with rhegmatogenous retinal detachment
- Age over 18 years with normal mental and psychological status
- Intraocular pressure less than 21 mmHg in both eyes before surgery
- No personal or family history of glaucoma
- Cup-to-disc ratio less than 0.5 in both eyes on fundus exam
- Understand the study purpose and sign informed consent
- High compliance with study requirements
You will not qualify if you...
- High intraocular pressure before surgery or glaucoma
- Acute or chronic systemic infections or blood diseases
- History of mental or psychological disorders
- Incomplete survey data or inability to cooperate
- Traumatic rhegmatogenous retinal detachment
- Active ocular infectious lesions in either eye
- Severe refractive media opacity affecting imaging
- History of congenital structural eye abnormalities
- Previous vitrectomy for other vitreoretinal diseases
- Considered unfit by researchers to participate in the trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The First Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality, China, 400042
Actively Recruiting
Research Team
H
Hui Peng
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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