search
Back to results

Bleb Vascularity Change After Subconjunctival Injection Bevacizumab

Primary Purpose

Bleb Vascularity, Conjunctival Scarring

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
bevacizumab
Sponsored by
Capital Medical University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bleb Vascularity focused on measuring bleb, vascular change, bevacizumab, trabeculectomy, Bleb vascularity associated with increased scarring activity, Conjunctival scarring finally leads to the obstruction of the fistula tract created by the filtering surgery, the recombinant human anti-VEGF antibody could inhibit angiogenesis of conjunctiva.

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Glaucoma patients after trabeculectomy whose bleb is hyperaemia

Exclusion Criteria:

  • Affected eye has normal IOP
  • Not allergic with Avastin

Sites / Locations

  • Tongren hospital

Outcomes

Primary Outcome Measures

bleb vascular change

Secondary Outcome Measures

Full Information

First Posted
December 29, 2008
Last Updated
December 29, 2008
Sponsor
Capital Medical University
search

1. Study Identification

Unique Protocol Identification Number
NCT00815594
Brief Title
Bleb Vascularity Change After Subconjunctival Injection Bevacizumab
Official Title
Bleb Vascularity Change After Subconjunctival Injection of Bevacizumab
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Unknown status
Study Start Date
December 2008 (undefined)
Primary Completion Date
March 2009 (Anticipated)
Study Completion Date
May 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Capital Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The occurrence of conjunctival scarring finally leads to the obstruction of the fistula tract created by the filtering surgery. Vascular endothelial growth factor is thought to be a key role in the formation of conjunctival scar, which play a pivotal role in the wound-healing process. So it seems that the recombinant human anti-VEGF antibody could inhibit angiogenesis, and reduce the conjunctival vascular formation in the wound-healing process after glaucoma filtering surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bleb Vascularity, Conjunctival Scarring
Keywords
bleb, vascular change, bevacizumab, trabeculectomy, Bleb vascularity associated with increased scarring activity, Conjunctival scarring finally leads to the obstruction of the fistula tract created by the filtering surgery, the recombinant human anti-VEGF antibody could inhibit angiogenesis of conjunctiva.

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
bevacizumab
Intervention Description
0.05ml, 1.25mg
Primary Outcome Measure Information:
Title
bleb vascular change
Time Frame
one day, one week, one month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Glaucoma patients after trabeculectomy whose bleb is hyperaemia Exclusion Criteria: Affected eye has normal IOP Not allergic with Avastin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liu Xuan, M.D.
Organizational Affiliation
An ophthalmologist in Tongren hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tongren hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China

12. IPD Sharing Statement

Learn more about this trial

Bleb Vascularity Change After Subconjunctival Injection Bevacizumab

We'll reach out to this number within 24 hrs