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NCT01446367 Clinical Trial

Corneal Changes After Retinal Surgery

Rhegmatogenous Retinal Detachment Clinical Trial

Official title:
Corneal Topographic Changes After 20-gauge Pars Plana Vitrectomy Associated With Scleral Buckling for the Treatment of Rhegmatogenous Retinal Detachment

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01446367
Other study ID # Cornea vs Vit-buckle
Secondary ID
Status Completed
Phase N/A
First received October 3, 2011
Last updated October 4, 2011
Start date February 2010
Est. completion date February 2011

Study information
Verified date October 2011
Source Universidade Federal do Paraná
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate the corneal changes after performing 20 gauge vitrectomy associated with scleral buckling for the treatment of rhegmatogenous retinal detachment.

Description:

Patients submitted to 20-gauge vitrectomy associated with scleral buckling were evaluated with corneal topography before surgery and in the 7,30 and 90 days after surgery to asses corneal curvature changes.

Recruitment information / eligibility
Status Completed
Enrollment 25
Est. completion date February 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients with rhegmatogenous retinal detachments

Exclusion Criteria:

- Previous eye surgery

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Universidade Federal do Paraná

References & Publications (1)

Weinberger D, Lichter H, Loya N, Axer-Siegel R, Muzmacher L, Gabbay U, Yassur Y. Corneal topographic changes after retinal and vitreous surgery. Ophthalmology. 1999 Aug;106(8):1521-4. — View Citation

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