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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00407108
Other study ID # APEC-005
Secondary ID
Status Withdrawn
Phase Phase 3
First received
Last updated
Start date March 2006
Est. completion date June 2006

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 Interventional

Clinical Trial Summary

To investigate the feasibility and advantages of using perfluorocarbon liquid (PCL) perfusion to remove vitreous during suction-cutting vitrectomy using a dual, dynamic drive (3D)technology. In complicated surgeries in advanced diabetic retinopathy and retinal detachment


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2006
Est. primary completion date March 2006
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Advanced diabetic retinopathy with retinal detachment Exclusion Criteria: - Retinal detachments of more than 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Vitrectomy


Locations

Country Name City State
Mexico Asociación para Evitar la Ceguera en Mexico, Hospital "Luis Sanchez Bulnes" Mexico City Mexico DF

Sponsors (1)

Lead Sponsor Collaborator
Asociación para Evitar la Ceguera en México

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Surgical time
Primary Facility of surgical maneuvers
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