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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00404209
Other study ID # APEC-008
Secondary ID
Status Terminated
Phase Phase 3
First received
Last updated
Start date March 2007
Est. completion date February 2008

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 pressurized perfluorocarbon liquid (PCL) perfusion to remove vitreous during suction-cutting 23 GA vitrectomy using a dual, dynamic drive (3D)technology, in complicated retinal detachment surgeries.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date February 2008
Est. primary completion date March 2007
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Complicated retinal detachment with no more than 6months of evolution Exclusion Criteria: - Retinal detachments of more than 6 months of evolution No light perception

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Vitrectomy
pressurized 23GA vitrectomy with a 3D system

Locations

Country Name City State
Mexico Asociación para Evitar la Ceguera en México, Hospital "Luis Sánchez 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 Perfluorocarbon liquids consumption two months
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