Influence of Intravitreal Aqueous Tamponade on Lens Status and Ocular
NCT ID: NCT06133660
Last Updated: 2023-11-15
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
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COMPLETED
21 participants
OBSERVATIONAL
2020-10-30
2023-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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PPV（pars plana vitrectomy） group
pars plana vitrectomy
pars plana vitrectomy and Silicone oil removal to distinguish subjects
Silicone oil removal group
pars plana vitrectomy
pars plana vitrectomy and Silicone oil removal to distinguish subjects
Interventions
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pars plana vitrectomy
pars plana vitrectomy and Silicone oil removal to distinguish subjects
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patients who underwent vitreous silicone oil tamponade and vitreous silicone oil removal due to various causes; ③ Intraoperative BSS was used for fill the vitreous cavity; ④ Before treatment, inform the patient that the clinical data may be used in clinical research, and the patient and his family are informed and sign the informed consent.
Exclusion Criteria
* intraoperative lens injury; ④ patients who refused to participate in the study.
16 Years
65 Years
ALL
No
Sponsors
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Bo Jia
OTHER
Responsible Party
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Bo Jia
M.D.
Locations
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The Second Hospital of Jilin University
Changchun, , China
Countries
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Other Identifiers
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second hospital of JilinU
Identifier Type: -
Identifier Source: org_study_id
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