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The innovative appliance of cohesive viscoelastic during pars plana vitrectomy in complicated ocular trauma

The innovative appliance of cohesive viscoelastic during pars plana vitrectomy in complicated ocular trauma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104657
Enrollment
Unknown
Registered
2025-06-20
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe traumatic eye injury (OTS=1 or 2)

Interventions

No use of cohesive viscoelastic in PPV group:None
Using of cohesive viscoelastic in PPV group:None

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Exposed Group Inclusion criteria:(1)Age between 18-65; (2) Gender unrestricted; (3) Patients diagnosed with severe traumatic ocular injury (OTS=1 or 2); (4) Patients diagnosed with PVR retinal detachment (Stage D2 or D3) and subjected to pars plana vitrectomy; (5) Use of viscoelastic agent for treatment. 2.Non-Exposed Group Inclusion criteria: (1)Age between 18-65; (2) Gender unrestricted; (3) Patients diagnosed with severe traumatic ocular injury (OTS=1 or 2); (4) Patients diagnosed with PVR retinal detachment (Stage D2 or D3) and subjected to pars plana vitrectomy; (5) No use of viscoelastic agent for treatment.

Exclusion criteria

Exclusion criteria: 1.Exposed Group Exclusion criteria: (1) Patients age above 65 or under 18; (2) Patients with visual acuity below the base line before injury. 2.Non-Exposed Group Exclusion criteria: (1) Patients age above 65 or under 18; (2) Patients with visual acuity below the base line before injury.

Design outcomes

Primary

MeasureTime frame
BCVA;

Countries

China

Contacts

Public ContactLiuxueying Zhong

Zhongshan Ophthalmic Center, Sun Yat-Sen University

843860477@qq.com+86 15099954411

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026