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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02876185
Other study ID # ICU_2015_39
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 8, 2016
Est. completion date May 5, 2023

Study information

Verified date October 2023
Source Fondation Ophtalmologique Adolphe de Rothschild
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Glaucoma is a progressive optical neuropathy, generally associated with ocular hypertension. The treatment aims to stabilize the visual field deficiencies by lowering the intraocular pressure. Due to the fluctuation of the visual field test and re-test measures, the European recommendations are to obtain 6 visual field tests in 2 years (or one every 4 months) in order to know if the pathology is progressing despite the current treatment (or if the treatment is necessary, in cases of intraocular hypertensions). The lack of ophthalmologists renders the monitoring of a beginning glaucoma, rarely compatible with the present recommendations. It is therefore crucial to evaluate new therapeutic alternatives, when faced to a decreasing medical demography and an increase the patient's needs. This study should allow to validate the possibility to delegate monitoring tasks to orthoptists during glaucoma surveillance. To organize the delegation of this surveillance to orthoptists would permit a better distribution of the ophthalmologist's activities.


Recruitment information / eligibility

Status Completed
Enrollment 133
Est. completion date May 5, 2023
Est. primary completion date May 5, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age from 18 years old or more - Open-angle glaucoma or ocular hypertension Exclusion Criteria: - Other active ocular pathology - Monophthalmic patients - Patients requiring a Goldmann visual field exam - Opposition of the patient to participate to the trial - Pregnant women or breastfeeding - Patient under juridical protection - Lack of affiliation to social security or universal health coverage

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Monitoring by an orthoptist then by an ophthalmologist
At each visit, the usual monitoring tests will be collected and viewed by the orthoptist then by the ophthalmologist concerning the necessity of an anticipated ophthalmological consultation

Locations

Country Name City State
France Centre hospitalier Angers
France Hôpital Ambroise-Paré Boulogne Billancourt
France Clinique Universitaire d'Ophtalmologie Grenoble
France Fondation Ophtalmologique A de Rothschild Paris

Sponsors (1)

Lead Sponsor Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary detection by the orthoptists of an abnormality that would require an anticipated ophthalmologic consultation 20 month of follow-up
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