NCT00407121

Brief Summary

Intravitreal injection of Bevacizumab in patients with Neovascular Membranes secondary to intraocular inflammation. We injected a single injection of Bevacizumab (2.5 mg/0.1 ml) and evaluate visual acuity , Fluorescein angiogram and retinal thickness by Optical Coherence Tomography (OCT) in 4 patients with Vogt Koyanagi Harada disease, 1 patient with Serpiginous Choroidopathy and 1 patient with Multifocal Choroiditis.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Dec 2006

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 1, 2006

Completed
Same day until next milestone

Study Start

First participant enrolled

December 1, 2006

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2006

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 4, 2006

Completed
Last Updated

May 30, 2024

Status Verified

May 1, 2024

Enrollment Period

Same day

First QC Date

December 1, 2006

Last Update Submit

May 29, 2024

Conditions

Keywords

Neovascular MembraneUveitisBevacizumab

Outcome Measures

Primary Outcomes (3)

  • Best corrected visual acuity

  • Retinal thickness by OCT

  • Leakage in Fluorescein angiogram

Interventions

Eligibility Criteria

Age25 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Clinical Diagnose
  • Patient Consent
  • Chronic stage of inflammation

You may not qualify if:

  • only eye
  • age lower than 30 yo.
  • Systemic condition

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Asociacion para Evitar la Ceguera en Mexico

Mexico City, Mexico City, 04030, Mexico

Location

MeSH Terms

Conditions

Uveomeningoencephalitic SyndromeWhite Dot SyndromesMultifocal ChoroiditisUveitis

Interventions

Bevacizumab

Condition Hierarchy (Ancestors)

Autoimmune Diseases of the Nervous SystemNervous System DiseasesUveal DiseasesEye DiseasesAutoimmune DiseasesImmune System DiseasesUveitis, PosteriorPanuveitisChoroiditisChoroid Diseases

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, HumanizedAntibodies, MonoclonalAntibodiesImmunoglobulinsImmunoproteinsBlood ProteinsProteinsAmino Acids, Peptides, and ProteinsSerum GlobulinsGlobulins

Study Officials

  • Veronica Kon-Jara, MD

    Asociación para Evitar la Ceguera en México

    PRINCIPAL INVESTIGATOR
  • LuzElena Concha-Del Rio, MD

    Asociación para Evitar la Ceguera en México

    STUDY CHAIR
0

Study Design

Study Type
interventional
Phase
phase 3
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 1, 2006

First Posted

December 4, 2006

Study Start

December 1, 2006

Primary Completion

December 1, 2006

Study Completion

December 1, 2006

Last Updated

May 30, 2024

Record last verified: 2024-05

Locations