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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01023009
Other study ID # APEC0006
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date May 2009
Est. completion date May 2010

Study information

Verified date May 2024
Source Asociación para Evitar la Ceguera en México
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

After an uneventfully small gauge vitrectomy we don´t think is necessary to occlude the eye for 24 hours


Recruitment information / eligibility

Status Terminated
Enrollment 50
Est. completion date May 2010
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - All patients with uneventful vitrectomy Exclusion Criteria: - Complicated vitrectomy or corneal lesion

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
vitrectomy


Locations

Country Name City State
Mexico Asociacion para Evitar la Ceguera en Mexico Mexico

Sponsors (1)

Lead Sponsor Collaborator
Asociación para Evitar la Ceguera en México

Country where clinical trial is conducted

Mexico, 

See also
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Terminated NCT02995746 - Intravitreal Dexamethasone Implant for Persistent Macular Thickening and Edema After Vitrectomy for Epiretinal Membrane N/A
Completed NCT03701542 - The Application of M-charts and Microperimetry for the Assessment of Visual Function in Patients After Vitrectomy Due to the Full Thickness Macular Hole.
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