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Clinical Trials/NCT02876185
NCT02876185
Completed
Not Applicable

Evaluation of the Possibility to Delegate Glaucoma Surveillance to Orthoptists in Hospital

Fondation Ophtalmologique Adolphe de Rothschild4 sites in 1 country133 target enrollmentApril 8, 2016
ConditionsGlaucoma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Glaucoma
Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Enrollment
133
Locations
4
Primary Endpoint
detection by the orthoptists of an abnormality that would require an anticipated ophthalmologic consultation
Status
Completed
Last Updated
last year

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
April 8, 2016
End Date
May 5, 2023
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

detection by the orthoptists of an abnormality that would require an anticipated ophthalmologic consultation

Time Frame: 20 month of follow-up

Study Sites (4)

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