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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT02486484
Date of registration: 24/05/2015
Prospective Registration: No
Primary sponsor: Rafic Hariri University Hospital
Public title: Ziv-aflibercept in Ocular Disease Requiring Anti-VEGF Injection Zaltrap
Scientific title: Phase 2 Ziv-aflibercept in Ocular Disease Short and Long-term Study
Date of first enrolment: March 2015
Target sample size: 100
Recruitment status: Unknown status
URL:  https://clinicaltrials.gov/show/NCT02486484
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).  
Phase:  Phase 2
Countries of recruitment
Lebanon
Contacts
Name:     Ahmad M Mansour, MD
Address: 
Telephone:
Email:
Affiliation:  Chair, Department of Ophthalmology, RHUH
Name:     Ahmad Mansour, MD
Address: 
Telephone: 9613377633
Email: ammansourmd@gmail.com
Affiliation: 
Name:     Ahmad M Mansour, MD
Address: 
Telephone: 9613377633
Email: ammansourmd@gmail.com
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria: All conditions that require anti-VEGF therapy

1. All eye conditions that require anti-VEGF therapy

2. Ability to understand and sign consent form

3. Ability to come for all follow-ups (2 year followup)

4. Acute form of the disease only in naïve cases

Exclusion Criteria:

1. Cardiovascular, cerebrovascular or peripheral vascular event less than 3 months prior
to enrollment

2. Current infection in the eye such as conjunctivitis or keratitis

3. Current upper respiratory tract infection

4. Fever or active body infection

5. Life-threatening disease with short survival

6. late presentation of the disease (chronic end stage disease of the eye)

7. Inability to sign informed consent

8. Inability to come for followups



Age minimum: N/A
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Macular Degeneration
Diabetic Retinopathy
Neovascularization
Choroidal Neovascularization
Cystoid Macular Edema
Retinal Neovascularization
Recurrent Pterygium
Retinal Vein Occlusion
Intervention(s)
Drug: ziv-aflibercept
Primary Outcome(s)
vision before and after ziv-aflibercept [Time Frame: 24 months]
Secondary Outcome(s)
central macular thickness before and after ziv-aflibercept [Time Frame: 24 months]
Secondary ID(s)
RaficHaririUH
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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