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Efficacy and safety of urokinase combined with conbercept or triamcinolone acetonide via intravitreal injection in the treatment for vitreous hemorrhage following various retinal disorders

Efficacy and safety of urokinase combined with conbercept or triamcinolone acetonide via intravitreal injection in the treatment for vitreous hemorrhage following various retinal disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015594
Enrollment
Unknown
Registered
2018-04-10
Start date
2018-05-09
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

dense vitreous hemorrhage following various retinal disease

Interventions

treatment group 1:intravitreal urokinase combined with triamcinolone acetonide
observation group:no interfere
treatment group 2:intravitreal injection of urokinase combined with conbercept

Sponsors

Xi'an 1st Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. VH by dilated pupil examination with funduscopy, presenting with no main retinal vessels /only optic nerve head visible possible; 2. VH in a single eye for 2-4 weekswith low visual acuity no more than 0.2; 3. VH in phakic eyes; 4. Patients with or without previous focal or grid macular laser treatments; 5. Intraocular pressure (IOP) below 21 mmHg by the measurement with tonometry; 6. Patients who are for the first time confirmed as having VH and undergo relevant treatments; 7. Aged over 40 years; 8. Irrespective of genders; 9. Provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with hemorrhages less than two weeks or more than four weeks from onset; 2. Patients with a specific allergy to any components of the relevant drugs; 3. Patients with a history of neuropathy or PPV surgery; 4. Patients with known coagulation dysfuntion or current use of anticoagulative medications other than aspirin; 5. Patients with uremia disease, a myocardial or cerebral vascular disease within one year duration, or hypertension with systolic pressure over 150 mmHg and/or diastolic pressure over 95 mmHg; 6. Patients with a history of diabetes mellitus, but fasting blood glucose is greater than 11.1mmol/l; 7. Patients with bilateral VHsignificant lens opacities, or diagnosis with any type of glaucoma; 8. Patients with a recent traumatic eye injury in the affected eye; 9. Concurrent retinal diseases detected by B-scan ultrasound at baseline, such as local vitreoretinal adhesion or traction, retinal detachment, or proliferation of the retina; and 10. Other VH after intraocular malignancy or no reason.

Design outcomes

Primary

MeasureTime frame
Best-corrected visual acuity;Degree of clearence of vitreous hemorrhage;intraocular pressure (IOP);

Countries

China

Contacts

Public ContactPerlin Lv

Xi'an 1st Hospital

1347116015@qq.com+86 13309250080

Outcome results

None listed

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