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Completed

NCT Number: NCT05271539

Intravitreal Ranibizumab Versus Its Combination With Dexamethasone in The Treatment of Diabetic Macular Edema

Intravitreal ranibizumab alone was Compared to adding dexamethasone to ranibizumab regarding central macular thickness, the visual acuity and the number of intravitreal injections needed to achieve the same effect on CMT and BCVA at the end of the 6 months duration of the study. Any significant change in final IOP, compared to baseline, in either group is reported.

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Key information

Age range

15 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Khaled G Abueleinen

Giza, Cairo Governorate, 12411, Egypt

About this study

This prospective randomized study measures the changes in central macular thickness, best corrected visual acuity and IOP in diabetic macular edema before and after the intravitreal injection of ranibizumab and dexamethasone, compared to ranibizumab alone, the current gold standard of care for diabetic macular edema.

Study participants were randomized into 2 groups: the first group received 3 Intravitreal injections of ranibizumab alone 1 month apart. While the second group received 1 Intravitreal injection of a combination of ranibizumab and 0.4 mg in 0.1 ml dexamethasone followed by 2 Intravitreal ranibizumab, 1 month apart (with dexamethasone if follow up OCT shows less than 10% improvement from baseline). Treatment was stopped when the treated eye achieved a central macular thickness of 250 microns or less with no focal parafoveal edema.

Final recorded central macular thickness in both groups compared to the baseline. By the end of the follow up period.

Final visual acuity was assessed in both groups compared to the baseline Change in final IOP, compared to baseline, in ranibizumab group and ranibizumab with dexamethasone group.

. The number of injections needed to achieve the same effect on CMT and BCVA.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diabetic macular edema with central macular thickness of 300 μm or greater (as measured by spectral domain optical coherence tomography [OCT]).
  • Best corrected visual acuity of 6/12 or less.

Exclusion criteria

  • ● History of any treatment for DME (including grid or focal laser photocoagulation) within the last 6 months
  • History of panretinal photocoagulation within the last 6 months.
  • PDR as indicated with Fluorescein Angiography as it will require PRP which may affect DME.
  • Macular ischemia, as indicated with Fluorescein Angiography.
  • Cataract surgery within three months or cataract that requires surgical intervention during the follow-up period.
  • Pseudophakia with Irvine Gass syndrome, as indicated with Fluorescein Angiography.
  • Vitreomacular traction syndrome.
  • Other causes of macular edema (eg. CRVO, CNV, uveitis, etc).
  • Glaucoma, whether suspected or confirmed.
  • Significant media opacity.
  • Patients with ocular or periocular infections, or infection in the other eye
  • Signs of Active or resolved uveitis and intraocular inflammation.
  • Bad diabetic control as indicated by HbA1C >8.
  • Renal impairment, hepatic impairment, or congestive heart failure.
  • History of cardiovascular insult or stroke.

Treatment and study plan

Lucentis alone group

Drug

The Lucentis alone group received 3 monthly intravitreal injections of lucentis alone or less than 3 injections if the central foveal thickness reached 250 microns

Lucentis dexamethasone group

Drug

Lucentis dexamethasone group received intravitreal injections of combination of both lucentis and commercial dexamethasone. the second group received monthly intravitreal injections of the same dose of ranibizumab combined with 0.4 mg in 0.1 ml dexamethasone (Dexamethasone sodium phosphate, Amriya Pharmaceuticals, Cairo, Egypt) in a separate 1ml syringe with 27- gauge × ½ inch sterile injection needle, followed by 2 Intravitreal ranibizumab, 1 month apart (with dexamethasone if follow up OCT shows less than 10% improvement from baseline i.e., PRN). Treatment was stopped when CMT improved below 250 µ.

Primary outcomes

  1. Central foveal thickness

    Time frame: 6 months after the first injection

    Central foveal thickness in microns measured by OCT

  2. BCVA (Decimal)

    Time frame: 6 months after the first injection

    Best corrected visual acuity measured on Snellen chart in Decimal form

  3. The number of injections

    Time frame: over 6 months duration of the study

    The total number of injections in each Arm group

Secondary outcomes

  1. IOP

    Time frame: 6 months after the first injection

    Intraocular pressure

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Comparative Study of the Efficacy of Intravitreal Ranibizumab Versus Its Combination With Commercial Dexamethasone in The Treatment of Diabetic Macular Edema

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Mar 9, 2022
Registry last updated
Mar 9, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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