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Effect of Intravitreal Anti-VEGF on Retinal Vessels Diameter

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ClinicalTrials.gov Identifier: NCT01626339
Recruitment Status : Unknown
Verified June 2012 by University of Malaya.
Recruitment status was:  Recruiting
First Posted : June 22, 2012
Last Update Posted : June 22, 2012
Sponsor:
Information provided by (Responsible Party):
University of Malaya

Brief Summary:

Patients who will be scheduled for intravitreal injection of Ranibizumab or Bevacizumab will be recruited in this prospective self-controlled trial. Fundus photography will carried out at baseline immediately before injection and at 3, 7 days and 30 days after the first injection. Using image analysis software, measurements summarized as the central retinal artery equivalent (CRAE) and central retinal vein equivalent (CRVE).

Null Hypothesis: There is no significant difference between arteriolar/venular diameter before and after injection of intravitreal ranibizumab/bevacizumab in the treated and untreated eye


Condition or disease Intervention/treatment
Age Related Macular Degeneration Drug: Intravitreal Ranibizumab Drug: Intravitreal bevacizumab

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Official Title: Effect of Intravitreal Anti-Vascular Endothelial Growth Factors on Retinal Vessels Diameter
Study Start Date : April 2012
Estimated Primary Completion Date : June 2012

Resource links provided by the National Library of Medicine

U.S. FDA Resources


Intervention Details:
    Drug: Intravitreal Ranibizumab
    Other Name: Lucentis
    Drug: Intravitreal bevacizumab
    Other Name: Avastin



Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

• Patients who wish and need bevacizumab or ranibizumab treatment for underlying disease

Exclusion Criteria:

  • History of previous systemic or ocular Anti-VEGF therapy
  • History of previous intravitreal injection with any drug
  • Intraocular pressure ≥ 22
  • Glaucoma
  • History or presence of thromboembolic events
  • Un-controlled blood pressure
  • Blood donation during the previous 3 weeks
  • Relevant media opacity of the lens

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01626339


Contacts
Contact: Mohammadreza Peyman, MD 0060173387260 ext 1 drmpeyman@yahoo.com
Contact: Visvaraja Subrayan, Prof d.visva@hotmail.com

Locations
Malaysia
University of Malaya Medical Center Recruiting
Kuala Lumpur, Malaysia, 59100
Contact: Mohammadreza Peyman, MD    0060173387260    drmpeyman@yahoo.com   
Sponsors and Collaborators
University of Malaya

Responsible Party: University of Malaya
ClinicalTrials.gov Identifier: NCT01626339     History of Changes
Other Study ID Numbers: PPUM/MDU/300/04/03
First Posted: June 22, 2012    Key Record Dates
Last Update Posted: June 22, 2012
Last Verified: June 2012

Keywords provided by University of Malaya:
Anti vascular endothelial growth factor
retinal vessels

Additional relevant MeSH terms:
Macular Degeneration
Retinal Degeneration
Retinal Diseases
Eye Diseases
Bevacizumab
Ranibizumab
Endothelial Growth Factors
Glucuronyl glucosamine glycan sulfate
Angiogenesis Inhibitors
Angiogenesis Modulating Agents
Growth Substances
Physiological Effects of Drugs
Growth Inhibitors
Antineoplastic Agents
Immunologic Factors
Anticoagulants
Hypolipidemic Agents
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Lipid Regulating Agents
Fibrinolytic Agents
Fibrin Modulating Agents
Hypoglycemic Agents