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Observation for treatment Patterns and Efficacy of Lucentis (Ranibizumab) in the Real clinical Applications in China

Observation for treatment patterns and efficacy with Lucentis (Ranibizumab) treatment in real life setting in approved indications in China

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022891
Enrollment
Unknown
Registered
2019-04-30
Start date
2018-10-31
Completion date
Unknown
Last updated
2019-05-05

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

Conditions

Age-Related Macular Degeneration/Diabetic Macular Edema/Macular Edema secondary to Retinal Vein Occlusion

Interventions

Case series:Ranibizumab

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Male or female patient = 18 years old; 2. Presence of visual impairment due to wAMD, DME and edema secondary to RVO; 3. Patients who are prescribed with ranibizumab, based on current approved indications; 4. Written informed consent.

Exclusion criteria

Exclusion criteria: 1. Simultaneous participation in a study that includes administration of any investigation drug or procedure; 2. Systemic treatment with any VEGF inhibitor in the 90 days prior to enrollment; 3. Ocular treatment with any VEGF inhibitor other than ranibizumab in the month prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Number of ranibizumab injections;Number of other intraocular injections;Number of visits;Time interval between injections;Number and reason of switching treatment;

Secondary

MeasureTime frame
Compare naiive patients and prior treated patients for the visual outcomes;Mean change of BCVA;Mean change of centraLretina thickness;Change of intraretinal fluid (IRF), subretinal fluid (SRF);Determine the relationship between injection number and VA improvement;Determine relationship between time period from the moment being diagnosed to first injection;Compare reimbursed/ non-reimbursed patients for the treatment pattern and visual;The safety objective of this study will be assessed based on the incidence rate, relationship and severity;

Countries

China

Contacts

Public ContactLin Lv

Zhongshan Ophthalmic Center, Sun Yat-sen University

lulin888@126.com+86 02066683995

Outcome results

None listed

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