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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03329976
Other study ID # KAUFFMANN PHRCI 2016
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 3, 2018
Est. completion date October 2026

Study information

Verified date March 2024
Source Centre Hospitalier Universitaire Dijon
Contact Yann KAUFFMANN, MD
Phone 3 80 29 51 73
Email yann.kauffmann@hotmail.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The prevalence of idiopathic epiretinal membranes (ERM) in people over 50 is estimated at 6 to 19%. Even though most cases show very few symptomats, they may induce alterations of the underlying retina and lead to visual impairment likely to greatly diminish quality of life in patients. Thanks to the ever-improving quality of vitreo-retinal surgery, ablation of these membranes is a frequent and safe procedure allowing a functional gain in the majority of cases. Given the increasing prevalence in the population concerned and the accelerated ageing of the lens after vitrectomy, cataract surgery is often associated with removal of the membrane. On the basis of a study in 142 patients, it was possible to identify clinical and morphological prognostic factors and to inclure them in a score to assess the chances of complete functional recovery at one year following the procedure . Age of the patient, the duration of symptoms, initial visual acuity and the quality of the junction between external and internal segments of photoreceptors in optic coherence tomography (OCT) appeared as significantly related to visual results. Using this score in a new prospective cohort would allow the investigators to make it a reliable and easy-to-use tool at the service of ophthalmologist surgeons and their patients and would provide scientific confirmation of the interest of earlier surgery in this disease. It would also allow the investigators to define in a validated and reproducible manner, a threshold for an ndication for ERM surgery, which is currently based on relatively subjective criteria mostly related to visual acuity.


Recruitment information / eligibility

Status Recruiting
Enrollment 450
Est. completion date October 2026
Est. primary completion date October 2026
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - Patients presenting idiopathic ERM visible on SD-OCT; - Indication for combined cataract and ERM surgery in a context of a fall in visual acuity or disabling metamorphopsia; - Patients who have provided verbal consent; - Age = 40 years. Exclusion Criteria: - Patients with secondary ERM (Diabetes WITH a history of diabetic retinopathy or maculopathy, occlusion of the retinal veins, uveitis intermediate/posterior uveitis or retinal tear/detachment in the studied eye; - Patient présentant toute autre maculopathie ou neuropathie optique ; - Patient presenting severe myopia (spherical equivalent = 6 diopters or axial length = 26 mm) ; - Patients presenting any other ophthalmological disease independent of the ERM and likely to limit visual acuity - Patients who have already undergone vitrectomy in the studied eye; - Non-visible or poorly visible fundus due to a cloudy vitreous (Signal on OCT Cirrus <5, Quality score on OCT Spectralis < 20, signal trend index on OCT Optovue < 30) - Patients without national health insurance cover - Pregnant or breast-feeding women.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
measurement of visual acuity
complete ophthalmologic examination of a macular SD-OCT, a fundus of eye, evaluation of the vision of contrasts (Pelli-Robson test) and quantification of metamorphopsies (M-Charts);

Locations

Country Name City State
France CHU Dijon Bourgogne Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary scale of monoyer at 5 meter over the 12 months of follow-up