CClinicalTrials.gg
CompletedNCT01315275LUDICUpdated Feb 23, 2017

A Clinical Study in Current Medical Practice of the Efficacy and Safety of Ranibizumab 0.5mg in Diabetic Patients Presenting a Visual Impairment Due to Macular Edema

A Phase 4 interventional study of Ranibizumab in Visual Impairment and Macular Edema, sponsored by Novartis Pharmaceuticals. Completed at 43 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-02-23.

Sponsored by Novartis Pharmaceuticals · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
394
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate the proportion of patients with a 10 letters gain on Best Corrected Visual Acuity (BCVA) at 6 months in current medical practice.

02

Conditions studied

  • Visual Impairment
  • Macular Edema

Keywords

  • visual impairment
  • macular edema
  • ranibizumab
  • visual impairment due to macular edema
03

In context

Vision Disorders

308 studies on the registry are indexed under Vision Disorders; 81 are open to participants now.

This study's enrollment of 394 is above the median of 66 across 211 interventional studies indexed under Vision Disorders.

Browse Vision Disorders studies →

Lead sponsor

Novartis Pharmaceuticals is the lead sponsor of 2,673 studies on the registry; 228 are open to participants now.

Of its 576 completed or terminated interventional studies of FDA-regulated products, 431 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male or female patients >18 years of age who have signed an informed consent
  • Patients with Type 1 or Type 2 diabetes mellitus (according to ADA or WHO guidelines) with HbA1c not more than 10.0% at screening (Visit 1). Patients should be on diet, exercise, and/or pharmacological treatment for diabetes.
  • Patients with visual impairment due to focal or diffuse DME in at least one eye
  • Central Retinal thickness on OCT ≥ 250 microns in the central subfield
  • BCVA score between 78 and 39 letters, inclusively, using ETDRS-like visual acuity testing charts at a testing distance of 4 meters (approximate Snellen equivalent of 20/32 to 20/160)
  • Decrease in vision is due to DME and not due to other causes, in the opinion of the investigator
  • Medication for the management of diabetes must have been stable within 3 months prior to randomization and is expected to remain stable during the course of the study.

Exclusion criteria

Exclusion Criteria:

Ocular concomitant conditions/ diseases

  • Concomitant conditions in the study eye which could, in the opinion of the investigator, prevent the improvement of visual acuity on study treatment
  • Active intraocular inflammation (grade trace or above) in either eye
  • Any active infection (e.g. conjunctivitis, keratitis, scleritis, uveitis, endophthalmitis) in either eye
  • History of uveitis in either eye Systemic conditions or treatments
  • Active systemic infection
  • History of stroke \< 3 months
  • Renal failure requiring dialysis or renal transplant OR renal insufficiency with creatinine levels > 2.0 mg/dl
  • Untreated diabetes mellitus
  • Blood pressure systolic > 160 mmHg and diastolic > 100 mmHg
  • Untreated hypertension
  • Known hypersensitivity to ranibizumab or any component of the ranibizumab formulation Others
  • Women of childbearing potential not using the contraception method(s) specified in this study (specify), as well as women who are breastfeeding

Other protocol-defined inclusion/exclusion criteria may apply

05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
394 participants (actual)

Study arms

  • Experimental
    Ranibizumab

    Drug: Ranibizumab

Interventions

  • DrugRanibizumab
06

What researchers measure

Primary outcomes

  1. proportion of patients with a 10 letters gain on Best Corrected Visual Acuity (BCVA)

    Time frame: 6 months

Secondary outcomes

  1. mean average change in BCVA from baseline

    Time frame: 6 months

  2. if the letters gain after 2 injections is predictive from the letters gain at 6 months

    Time frame: 6 months

  3. mean number of injections needed to obtain a 10 letters gain

    Time frame: 6 months

  4. mean number of injections needed to obtain a stable visual acuity for three consecutive monthly assessments

    Time frame: 6 months

  5. efficacy of ranibizumab IVT on Central Retinal Thickness (OCT)

    Time frame: 6 months

07

Study locations

43 sites
  • Novartis Investigative Site
    Amiens, 80054, France
  • Novartis Investigative Site
    Angers, 49044, France
  • Novartis Investigative Site
    Besançon cedex, 25030, France
  • Novartis Investigative Site
    Bobigny, 93009, France
  • Novartis Investigative Site
    Bordeaux, 33000, France
  • Novartis Investigative Site
    Bordeaux, 33100, France
  • Novartis Investigative Site
    Caen, 14050, France
  • Novartis Investigative Site
    Cesson Sevigne, 35510, France
  • Novartis Investigative Site
    Clermont-ferrand, 63014, France
  • Novartis Investigative Site
    Créteil, 94000, France
  • Novartis Investigative Site
    Grenoble, 38000, France
  • Novartis Investigative Site
    Lille, 59037, France
  • Novartis Investigative Site
    Lyon Cedex 04, 69317, France
  • Novartis Investigative Site
    Lyon, 69007, France
  • Novartis Investigative Site
    Lyon, 69275, France
  • Novartis Investigative Site
    Lyon, 69437, France
  • Novartis Investigative Site
    Mantes la joile, 78201, France
  • Novartis Investigative Site
    Marseille cedex 05, 13385, France
  • Novartis Investigative Site
    Marseille, 13008, France
  • Novartis Investigative Site
    Melun, 77000, France
  • Novartis Investigative Site
    Montpellier, 34000, France
  • Novartis Investigative Site
    Montpellier, 34295, France
  • Novartis Investigative Site
    Nice, 06000, France
  • Novartis Investigative Site
    Nimes, 30029, France
  • Novartis Investigative Site
    Osny, 95520, France
  • Novartis Investigative Site
    Paris Cedex 19, 75940, France
  • Novartis Investigative Site
    Paris, Cedex 12, F-75571, France
  • Novartis Investigative Site
    Paris, 75006, France
  • Novartis Investigative Site
    Paris, 75007, France
  • Novartis Investigative Site
    Paris, 75015, France
  • Novartis Investigative Site
    Puilboreau, 17138, France
  • Novartis Investigative Site
    Reims, 51092, France
  • Novartis Investigative Site
    Rouen, 76100, France
  • Novartis Investigative Site
    Saint Brieuc, 22015, France
  • Novartis Investigative Site
    Saint Etienne, 42000, France
  • Novartis Investigative Site
    Saitnt Herblain, 44819, France
  • Novartis Investigative Site
    St Jean, 31240, France
  • Novartis Investigative Site
    St-Priest-en-Jarez, 42270, France
  • Novartis Investigative Site
    Strasbourg, 67000, France
  • Novartis Investigative Site
    Toulouse, 31077, France
  • Novartis Investigative Site
    Tours, 37044, France
  • Novartis Investigative Site
    Vandoeuvre les Nancy, 54511, France
  • Novartis Investigative Site
    Vannes, 56000, France
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 23, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01315275
Lead sponsor
Novartis Pharmaceuticals
Responsible party
Sponsor
First posted
Mar 15, 2011
Start date
Feb 2011
Primary completion
Aug 2012
Completion
Aug 2012
Last update
Feb 23, 2017

Study contacts

Novartis Pharmaceuticals
study director · Novartis Pharmaceuticals
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion