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A prospective, controlled clinical trial of pharmacokinetics following subretinal and intravitreous anti-VEGF treatment

A prospective, controlled clinical trial of pharmacokinetics following subretinal and intravitreous anti-VEGF treatment

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-17011519
Enrollment
Unknown
Registered
2017-05-30
Start date
2017-06-01
Completion date
Unknown
Last updated
2017-06-05

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

Conditions

diabetic retinopathy

Interventions

Test Group 1:vitrectomy with saline tamponade and subretinal anti-VEGF injection
Test Group 2:vitrectomy with saline tamponade and intravitreous anti-VEGF injection
Test Group 3:vitrectomy with silicone oil tamponade and intravitreous anti-VEGF injection
Test Group 4:vitrectomy with gas tamponade and intravitreous anti-VEGF injection
Blank Group:intravitreous anti-VEGF injection

Sponsors

Shanghai Jiaotong University Affiliated Ninth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. aged 30 to 90 years patient male or female ; 2. subjects were not treated with anti-VEGF drugs; 3. subjects with diabetic retinopathy; 4. indicated for vitrectomy (unabsorbed or recrudescent vitreous hemorrhage, retinal detachment); 5. patients are voluntarily involved in this clinical trial and signed informed consent; 6. abide by follow-up visit according to the plan schedule;

Exclusion criteria

Exclusion criteria: 1. researchers consider who are not eligible for inclusion; 2. severe systemic diseases that may affect the results (heart failure, respiratory failure neuropathy, mental disorders, hematological disorders, immune diseaseInfectious diseases, malignant tumors and organ transplantation); 3. vitrectomy for other reasons except diabetic retinopathy; 4. history of orbital surgery; orbital deformity, trauma patients; uveitis eye, anterior chamber inflammation, keratitis, corneal degeneration.

Design outcomes

Primary

MeasureTime frame
concentration of anti-VEGF fusion protein;

Countries

China

Contacts

Public ContactZhaoyang Wang

Shanghai Jiaotong University Affiliated Ninth People's Hospital

Zhaokekewzy@hotmail.com+86 15921108602

Outcome results

None listed

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