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Comparison of subretinal versus intravitreal injection of tissue type plasminogen activator combined with conbercept and C3F8 in the treatment of acute macular hemorrhage

Comparison of subretinal versus intravitreal injection of tissue type plasminogen activator combined with conbercept and C3F8 in the treatment of acute macular hemorrhage

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089058
Enrollment
Unknown
Registered
2024-08-30
Start date
2023-04-17
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

submacular hemorrhage

Interventions

Intravitreal injection group:Intravitreal injection of Conbercept (0.5mg/0.05ml) + tissue type plasminogen activator (25ug)+C3F8 gas 0.4ml
Subretinal injection group:Vitrectomy and subretinal injection of tissue type plasminogen activator (25ug), and intravitreal injection of conbercept (0.5mg/0.05ml)++C3F8 gas 0.4ml

Sponsors

Dongguan Guangming Ophthalmology Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age above 45 years old; 2. SMH with a duration of no more than 2 weeks from onset to surgery; 3. Diagnosed as wAMD or PCV based on fundus photography, FFA combined with ICGA examination; 4. The thickness of subretinal hemorrhage involving the macular fovea is greater than 125um (SD-OCT scan), and the diameter exceeds 1PD size.

Exclusion criteria

Exclusion criteria: 1. Subretinal hemorrhage in the macular area caused by factors other than dehumidifying age-related macular degeneration and PCV; 2. Individuals with a history of cerebral infarction, cerebral ischemia, or myocardial infarction within 6 months; 3. Those who have had previous vitrectomy surgery or macular degeneration causing scars; 4. Patients who use anticoagulants; 5. People with diabetes retinopathy, uveitis and high myopia; 6. Those who cannot maintain a face down position; 7. Patients with refractive interstitial opacity that affects fundus observation.

Design outcomes

Primary

MeasureTime frame
Displacement and absorption of SMH;visual acuity;central PED thickness;Central retinal thickness;Intraocular pressure;

Countries

China

Contacts

Public ContactQing Lian

Dongguan Guangming Ophthalmology Hospital

lianqing5678@163.com+86 181 3591 1081

Outcome results

None listed

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