PASCAL: Safety and Complications, Experience After 1301 Consecutive Cases

Bruch Rupture Clinical Trial

Official title:

Pattern Scan Laser Photocoagulation: Safety and Complications, Experience After 1301 Consecutive Cases.

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00803153
• Other study ID #: APEC-038
• Status: Withdrawn
• Start date: December 2008
• Est. completion date: December 2008

Study information

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

Clinical Trial Summary

To report the safety and incidence of adverse effects, during and after a successful photocoagulation for different pathologies using a Pattern Scan Laser (PASCAL) system and its modified settings

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2008
• Est. primary completion date: December 2008
• Accepts healthy volunteers: No
• Gender: All
• Age group: 10 Years to 90 Years

Eligibility

Inclusion Criteria:

• Patients treated with PASCAL system

Exclusion Criteria:

• Uncompleted file.

• Loss of follow-up.

Related Conditions & MeSH terms

• Bruch Rupture
• Choroidal Detachment
• Choroidal Effusions
• Rupture

Intervention

Procedure:
• Panretinal Photocoagulation [Pattern Scan Laser (PASCAL) system]

Locations

Country	Name	City	State
Mexico	Asociación para Evitar la Ceguera en México	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	Complication rates		during treatment and follow-up