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Analysis of Risk Factors for High Intraocular Pressure and Retinal Detachment Recurrence After Vitrectomy with Silicone Oil Tamponade in Retinal Detachment Patients

Analysis of Risk Factors for High Intraocular Pressure and Retinal Detachment Recurrence After Vitrectomy with Silicone Oil Tamponade in Retinal Detachment Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097137
Enrollment
Unknown
Registered
2025-02-13
Start date
2024-09-01
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Retinal Detachment

Interventions

Group 1:Intraocular pressure and retinal condition were measured and recorded at postoperative day 1, week 1, month 1, month 3, month 6, and before silicone oil removal surgery, with cases of elevated
Group 2:Intraocular pressure and retinal condition were measured and recorded at postoperative day 1, week 1, month 1, month 3, month 6, and before silicone oil removal surgery, with no cases of eleva

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosed with "rhegmatogenous retinal detachment"; 2. Aged over 18 years old, with normal mental and psychological status, regardless of gender; 3. Intraocular pressure of both eyes is less than 21 mmHg before surgery, and having no personal or family history of glaucoma; 4. Cup - to - disc ratio (C/D) in fundus examination is less than 0.5 for both eyes; 5. Those who understand the purpose of this study, sign the "Informed Consent Form" and have a high degree of compliance.

Exclusion criteria

Exclusion criteria: 1. Those with high intraocular pressure before surgery and suffering from ophthalmic diseases such as glaucoma; 3. Those with acute or chronic systemic infections and hematological diseases; 4. Those with a history of mental and psychological diseases; 5. Those with incomplete survey data or unable to cooperate with this research; 5. Those with traumatic rhegmatogenous retinal detachment; 6. Those with active ocular infectious lesions in either eye; 7. Those with severe refractive media opacity (such as corneal nebula, corneal leukoma) in the target eye, which affects imaging examinations during postoperative follow - up; 8. Those with a history of congenital structural abnormalities in the target eye; 9. Those who have undergone vitrectomy for other vitreoretinal diseases in the target eye before screening; 10. Those whom the researchers consider unfit to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
intraocular pressure;retinal detachment condition;Wide - angle fundus photography;

Countries

China

Contacts

Public ContactHui Peng

The First Affiliated Hospital of Chongqing Medical University

pengh9@sina.com+86 130 7236 9950

Outcome results

None listed

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