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Long-term prognosis of w-AMD patients with sichuan medical insurance group after injection of compassip (panda study)

Long-term prognosis of w-AMD patients with sichuan medical insurance group after injection of compassip (panda study)

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017606
Enrollment
Unknown
Registered
2018-08-06
Start date
2017-08-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

w-AMD

Interventions

Case series:compassip

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Sign informed consent and be willing to provide visitation data in accordance with the data collection content specified in the test; 2. The target eye must meet the following requirements:Active choroidal neovascularization (CNV) lesions secondary to primary or recurrent central fovea and paracentricular fovea in w-amd,The criteria for judging active CNV are as follows: (1) Fresh bleeding; (2) Neuroepithelial detachment on OCT; (3) Leaking on fluorescein; 3. It can be photographed by color under the eye, fundus autofluorescence(FAF), OCT and FFA can be used to observe fundus; 4. best corrected visual acuity(BCVA) more than 20 letters(contains 20 letters); 5. Treatment expenses can be included in sichuan medical insurance catalog reimbursement.

Exclusion criteria

Exclusion criteria: 1. The investigator determined that the existing or previous non exudability AMD disease in the target eye seriously affected the detection of fundus or central vision, and best corrected visual acuity (BCVA) was less than 20 letters; 2. The target eye received PDT treatment within 6 months prior to screening or the target eye received medication for CNV within 6 months prior to screening (such as Ranibizumab, Bevacizumab injection, TA, Steroid etc.), or non target eyes were treated with VEGF drugs within 1 months before screening; 3. The target eye has received intraocular surgery within 3 months(retinal photocoagulation etc.), an eye operation had been received within 1 months(such as Eyelid surgery, pterygium surgery etc.); 4. Active eye infection of the target eye or the contralateral eye(such as Blepharitis, infectious conjunctivitis, keratitis, sclera, endophthalmitis); 5. Have a history of anaphylaxis or allergies to fluorescein sodium and ICG, and have a history of treating or diagnosing protein product.Have a history of allergies to treatment or diagnosis of protein products; 6. The target eye cannot complete two consecutive visits within 6 months; 7. The investigators say the need to exclude.

Design outcomes

Primary

MeasureTime frame
best corrected visual acuity;

Countries

China

Contacts

Public ContactMing Zhang

West China Hospital, Sichuan University

zhangmingscu@126.com+86 18980602122

Outcome results

None listed

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