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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03793400
Other study ID # 180916
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 13, 2018
Est. completion date December 28, 2018

Study information

Verified date January 2019
Source Changhua Christian Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the long-term outcome of active choroidal neovascularization (CNV) in punctate inner choroidopathy (PIC) or multifocal choroiditis (MFC) after anti-vascular endothelial factor treatment.


Description:

To evaluate the long-term outcome of active choroidal neovascularization (CNV) in punctate inner choroidopathy (PIC) or multifocal choroiditis (MFC) after anti-vascular endothelial factor treatment.

The age, sex, best corrected visual acuity (BCVA) in Snellen chart, and refractive status for each patient were recorded. All patients had thorough clinical examinations, including slit lamp biomicroscopy, indirect ophthalmoloscopy, and spectral domain optical coherence tomography during each visit. Fundus photography, fluorescein angiography, and indocyanine angiography were performed on all patients. OCT angiography was performed.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date December 28, 2018
Est. primary completion date April 13, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. Patients were punctate inner choroidopathy or multifocal choroiditis with active choroidal neovascularization.

2. Follow up over 4 years.

Exclusion Criteria:

1. Patients were not punctate inner choroidopathy or multifocal choroiditis with active choroidal neovascularization

2. Patients were punctate inner choroidopathy or multifocal choroiditis with active choroidal neovascularization but loss follow over 1 year.

Study Design


Intervention

Drug:
Bevacizumab Injection
Anti-vascular endothelial growth factor (VEGF)

Locations

Country Name City State
Taiwan Changhua Christian Hospital Changhua

Sponsors (1)

Lead Sponsor Collaborator
Changhua Christian Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Wilcoxon Signed-Rank test A statistical comparison of average of two dependent samples Baseline,48 month.
Secondary visual acuity visual acuity in logMAR Baseline,48 month.
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