Effectiveness of Anti-VEGF Treatments in Wet AMD in Active Smokers

Sponsor
Brugmann University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04685369
Collaborator
(none)
148
1
8.5
17.3

Study Details

Study Description

Brief Summary

" Wet Age-related Macular Degeneration (wet AMD)" is characterized by the appearance of new choroidal vessels. Several clinical studies have shown the effectiveness of intra-vitreous injections of anti-VEGF (bevacizumab, ranibizumab and aflibercept) against these choroidal neovessels. However, some eyes appear to respond less well or be resistant to anti-VEGF injections, which affects visual acuity. To improve the clinical management of patients with wet AMD, it is important to be able to determine which factors determine the response to anti-VEGF treatment.

Non-modifiable factors such as visual acuity or the patient's age at the time of the first injections, the type and size of choroidal neovascularization, as well as certain genetic polymorphisms are known. Two studies, one carried out in Korean patients, the other in different centers in Singapore, New Zealand, Australia and Switzerland showed that active smoking was associated with a poorer response to intra-vitreous injections of ranibizumab, since smoking is also an already well-known modifiable risk factor for the onset of AMD. Another study in the Netherlands shows a poorer visual prognosis after five years of injection treatment in patients who smoke.

This study aims to study the effect of active smoking on the visual prognosis of patients with exudative AMD and treated with anti-VEGF injections in a Belgian cohort.

Condition or Disease Intervention/Treatment Phase
  • Other: Medical Data extraction

Study Design

Study Type:
Observational
Actual Enrollment :
148 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Effectiveness of Anti-VEGF Treatments in Wet AMD in Active Smokers
Actual Study Start Date :
Nov 10, 2020
Actual Primary Completion Date :
Jul 28, 2021
Actual Study Completion Date :
Jul 28, 2021

Arms and Interventions

Arm Intervention/Treatment
Active smokers with wet AMD

Other: Medical Data extraction
Medical Data extraction

Outcome Measures

Primary Outcome Measures

  1. Monoyer chart result [Baseline]

    Best corrected visual acuity using a monoyer chart - data collected on one eye only. Monoyer charts are planks with letters displayed: the letters in each row are the same size and the size increases as you go down.

  2. Monoyer chart result [4 months after baseline]

    Best corrected visual acuity using a monoyer chart - data collected on one eye only. Monoyer charts are planks with letters displayed: the letters in each row are the same size and the size increases as you go down.

Secondary Outcome Measures

  1. Central macular thickness [Baseline]

    Central macular thickness measured by optical coherence tomography at baseline examination

  2. Central macular thickness [4 months after baseline]

    Central macular thickness measured by optical coherence tomography at final examination

  3. Pigment epithelial detachment [Baseline]

    Morphological analysis of the retinal pigment epithelium on optical coherence tomography (OCT), to assess presence or absence of detachment at baseline visit.

  4. Sub-retinal fluid [Baseline]

    Morphological analysis of retinal layers on optical coherence tomography (OCT), to assess presence or absence of sub-retinal fluid at baseline visit.

  5. Choroidal neovascularization subtype [Baseline]

    Morphological analysis of fluorescein angiography, to assess the type of choroidal neovascularization at baseline visit.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • CHU Brugmann Hospital patients

  • Patients who received three intra-vitreous injections of ranibizumab, aflibercept or bevacizumab 4 weeks apart as the first intra-vitreous treatment between January 2016 and December 2020.

  • Visual acuity measured before the start of the injections (maximum 1 month) and after the series of three injections (4 to 8 weeks after the last injection)

  • Patients whose smoking status is known and for whom the following history appears: hypertension, diabetes, taking anti-coagulants or anti-aggregants.

Exclusion Criteria:
  • Patients who have already received another intravitreal treatment in the past.

  • Patients who have been treated with dynamic phototherapy before or at the same time as the injections.

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Brugmann Brussels Belgium 1020

Sponsors and Collaborators

  • Brugmann University Hospital

Investigators

  • Principal Investigator: Sophie Caspers, CHU Brugmann

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Laurence Postelmans, Head of ophtalmology department, Brugmann University Hospital
ClinicalTrials.gov Identifier:
NCT04685369
Other Study ID Numbers:
  • CHUB-Caspers
First Posted:
Dec 28, 2020
Last Update Posted:
Mar 8, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 8, 2022