NCT02304068

Brief Summary

Currently the best treatment for "wet" macular degeneration involves regular injections of Ranibizumab (Lucentis). In the initial clinical trials, the drug was injected into the eye every month. Since then a number of studies have found similar benefits when the drug is given with a fixed number of injections initially and then with further injections only when needed. This approach has been adopted in the UK, following recommendation by the National Institute for Clinical Excellence (NICE). Although this approach reduces the expense and risk of un-necessary treatment, it does require regular hospital assessment of disease activity to determine if a repeat injection is required or can be deferred. The hospital assessment is time-consuming, inconvenient and the large number of assessments can cause delays in hospital follow-up. Using three different assessment criteria to monitor disease activity at home, the investigators plan to see if home monitoring is as good as hospital assessment. The investigators have already identified that many patients dislike the lengthy hospital assessment visit and would welcome the opportunity to do some of the monitoring of disease activity at home. The investigators have also shown that they understand and can complete each of the home assessment tests. In this pilot project, the investigators aim to get an idea of how reliable home monitoring can be in a small sample of just over 30 patients. The data that the pilot project generates will be used to influence and to help plan a subsequent, larger, national study to be submitted for funding to the National Institute for Health Research.

Trial Health

100
On Track

Trial Health Score

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

Timeline
Completed

Started Apr 2012

Shorter than P25 for not_applicable

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2012

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2012

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

November 4, 2014

Completed
27 days until next milestone

First Posted

Study publicly available on registry

December 1, 2014

Completed
Last Updated

August 20, 2019

Status Verified

August 1, 2019

Enrollment Period

6 months

First QC Date

November 4, 2014

Last Update Submit

August 16, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • Monitor disease activity at home using near reading chart

    The reproducibility of the home monitoring assessment exercise

    7 months

Study Arms (1)

Intra-vitreal injection

OTHER
Other: Home monitoringOther: Hospital assessment

Interventions

Intra-vitreal injection
Intra-vitreal injection

Eligibility Criteria

Age60 Years - 99 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients over 60 years with a clinical diagnosis of neovascular age-related macular degeneration (ARMD), receiving treatment with intra-vitreal ranibizumab in accordance with current UK practice
  • At least 6 months of prior treatment beyond the loading phase of three fixed injections
  • At least 2 injections during the prior 6 months of the maintenance phase of treatment
  • Early Treatment for Diabetic Retinopathy Study (ETDRS) chart letter score at 2m of between 30 and 70 letters at the start of the study

You may not qualify if:

  • Patients with chronic intra-retinal cycts or sub-retinal fluid in the study eye on Optical coherence tomography (OCT) examination despite prior treatment and judged to be stable without the need for further treatment
  • Significant hearing impairment, felt likely to interfere with training and the telephone calls prior to the home monitoring
  • Lack of informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Blood Glucose Self-Monitoring

Intervention Hierarchy (Ancestors)

Blood Chemical AnalysisClinical Chemistry TestsClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisDiagnostic Techniques, EndocrineMonitoring, PhysiologicSelf-TestingSelf CareTherapeuticsInvestigative Techniques

Study Design

Study Type
interventional
Phase
not applicable
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 4, 2014

First Posted

December 1, 2014

Study Start

April 1, 2012

Primary Completion

October 1, 2012

Study Completion

October 1, 2012

Last Updated

August 20, 2019

Record last verified: 2019-08