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Effect on the Vitreous of the Not Complicated Surgery of the Cataract to the Emmetropic Patient (VITRECAT)

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ClinicalTrials.gov Identifier: NCT02783209
Recruitment Status : Terminated (Major difficulties of patient inclusions)
First Posted : May 26, 2016
Last Update Posted : February 5, 2018
Sponsor:
Information provided by (Responsible Party):
Fondation Ophtalmologique Adolphe de Rothschild

Study Description
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Brief Summary:
This study evaluates the association between surgery of the cataract and posterior vitreous detachment, in the emmetropic patient, by comparing eyes operated with eyes not operated in the same group of patients

Condition or disease Intervention/treatment Phase
Cataract Vitreous Detachment Procedure: Cataract surgery Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 30 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Other
Official Title: Effect on the Vitreous of the Not Complicated Surgery of the Cataract to the Emmetropic Patient
Actual Study Start Date : December 2014
Actual Primary Completion Date : February 1, 2018
Actual Study Completion Date : February 1, 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cataract

Arms and Interventions
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Arm Intervention/treatment
Cataract surgery
Patient acts as his own control
 Procedure: Cataract surgery


Outcome Measures
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Primary Outcome Measures :
  1. Occurence of vitreous detachment in the operated eye [ Time Frame: 3 months after the cataract surgery ]

Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adult emmetropic patient
  • Without complete posterior vitreus detachment in both eyes before having surgery.

Exclusion Criteria:

  • Diabetic retinopathy
  • Ophthalmological treatment in progress
  • History of ophthalmological surgery
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02783209


Locations
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France
URC Fondation Ophtalmologique A de Rothschild
Paris, France, 75019
Sponsors and Collaborators
Fondation Ophtalmologique Adolphe de Rothschild
More Information
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Responsible Party: Fondation Ophtalmologique Adolphe de Rothschild
ClinicalTrials.gov Identifier: NCT02783209    
Other Study ID Numbers: FME_2014_5
First Posted: May 26, 2016    Key Record Dates
Last Update Posted: February 5, 2018
Last Verified: February 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Cataract
Vitreous Detachment
Lens Diseases
Eye Diseases