Evaluation of Intraoperative Slow-release Dexamethasone Implant for Epiretinal Membrane

Sponsor
Peking University People's Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05416827
Collaborator
(none)
30
2
3

Study Details

Study Description

Brief Summary

Epiretinal membrane (ERM) is a commonly encountered vitreoretinal interface anomaly with a prevalence of approximately 10% in the adult population. It is often treated with pars plana vitrectomy (PPV) and membrane peeling when symptomatic. PPV is generally successful at improving visual acuity (VA) and/or metamorphopsia. At times, however, visual recovery can be hindered by macular edema in the post-vitrectomy period. Ozurdex can accelerate the resorption of intraretinal edema and hasten the improvement in the visual acuity. It has been shown to facilitate fluid absorption by both stimulating endogenous adenosine signaling in Muller cells and by down regulating vascular endothelial growth factor production. So, this study aim to investigate the efficacy of Ozurdex implant after PPV in epiretinal membrane eyes.

Condition or Disease Intervention/Treatment Phase
  • Procedure: slow-release dexamethasone implant
N/A

Detailed Description

Small gauge pars plana vitrectomy (PPV) with membrane peeling is used to successfully treat macular epiretinal membranes (ERMs) with a postoperative improvement of visual acuity in the majority of cases. Traditionally, the treatment of ERMs has been performed purely by peeling the membrane mechanically and then waiting for the intraretinal edema to resolve spontaneously. In the last few years, some publications raised the possibility that triamcinolone acetonide (TA),given as an intravitreal injection at the end of surgery, can accelerate the resorption of intraretinal edema and hasten the improvement in the visual acuity. It has been shown to facilitate fluid absorption by both stimulating endogenous adenosine signaling in Muller cells and by down regulating vascular endothelial growth factor production. Dexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs that has anti-inflammatory and immunosuppressant activity 30 times that of cortisol and 6 times that of triamcinolone. As the postoperative cystoid macular edema usually peaks 4 to 6 weeks after surgery the difference in the half life can be significant and explained the results in past publications. While the use of intravitreal TA as an adjuvant to PPV with membrane peel showed conflicting results. Only few publications demonstrated the effectiveness of Ozurdex in the treatment of macular edema in a vitrectomized eye, after ERM removal.So, this study aim to investigate the efficacy of Ozurdex implant after PPV in epiretinal membrane eyes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Evaluation of Intraoperative Slow-release Dexamethasone Implant Used During Vitrectomy for Epiretinal Membrane
Anticipated Study Start Date :
Jun 15, 2022
Anticipated Primary Completion Date :
Sep 15, 2022
Anticipated Study Completion Date :
Sep 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: PPV group

Epiretinal membrane eyes underwent PPV

Procedure: slow-release dexamethasone implant
Epiretinal membrane eyes underwent PPV combined with Ozurdex implant

Experimental: PPV+implant Group

Epiretinal membrane eyes underwent PPV combined with Ozurdex implant

Procedure: slow-release dexamethasone implant
Epiretinal membrane eyes underwent PPV combined with Ozurdex implant

Outcome Measures

Primary Outcome Measures

  1. CMT [from preoperation to 3 months follow-up]

    central macular thickness

  2. IOP [from preoperation to 3 months follow-up]

    intraocular pressure

  3. BCVA [from preoperation to 3 months follow-up]

    best-corrected visual acuity

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients with a visually significant (BCVA<20/50) idiopathic epiretinal membrane.

  • ocular axial length less than 27.00 mm (optical biometry) associated with cataracts.

Exclusion Criteria:
  • concomitant or previous macular diseases (diabetic macular edema, retinal vein occlusion and agerelated macular degeneration).

  • secondary epiretinal membrane, other visually significant macular pathology and prior intravitreal triamcinolone acetonide injection.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Peking University People's Hospital

Investigators

  • Study Chair: Jinfeng Qu, MD, Peking University People's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Peking University People's Hospital
ClinicalTrials.gov Identifier:
NCT05416827
Other Study ID Numbers:
  • PKUPHophthal
First Posted:
Jun 13, 2022
Last Update Posted:
Jun 13, 2022
Last Verified:
Jun 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
Keywords provided by Peking University People's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 13, 2022