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NCT01478763 Clinical Trial

Vitrous Analysis in Proliferative Diabetic Retinopathy

Proliferative Diabetic Retinopathy Clinical Trial

Official title:
Analysis of Vitreous Proteins in Patients Undergoing Pars Plana Vitrectomy for Proliferative Diabetic Retinopathy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01478763
Other study ID # Vitreous1
Secondary ID
Status Completed
Phase N/A
First received November 21, 2011
Last updated September 24, 2014
Start date January 2011
Est. completion date September 2014

Study information
Verified date September 2014
Source St. Erik Eye Hospital
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Observational

Clinical Trial Summary

Analysis of vitreous proteins in patients undergoing pars plana vitrectomy for proliferative diabetic retinopathy

Description:

To analyse and compare vitreous proteins in patients undergoing pars plana vitrectomy for proliferative diabetic retinopathy.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group 12 Years and older
Eligibility Inclusion Criteria:

- proliferative diabetic retinopathy with vitreous hemorrhage

Exclusion Criteria:

- vitreous hemorrhage of other cause than proliferative diabetic retinopathy

- previous vitrectomy

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden St. Erik Eye Hospital Stockholm NonUS

Sponsors (1)
Lead Sponsor Collaborator
Anders Kvanta

Country where clinical trial is conducted

Sweden, 

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Completed NCT00446381 - Effect of Macugen(Pegaptanib)on Surgical Outcomes and VEGF Levels in Diabetic Patients With PDR (Diabetic Retinopathy or CSDME (Macular Edema) N/A
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