Macular Detachment Associated With Intrachoroidal Cavitation

Macular Detachment Clinical Trial

Official title:

Macular Detachment Associated With Intrachoroidal Cavitation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01959724
• Other study ID #: Kyorineye012
• Secondary ID: Kyorineye12
• Status: Completed
• Phase: N/A
• First received: October 7, 2013
• Last updated: October 8, 2013
• Start date: April 2007
• Est. completion date: September 2013

Study information

• Verified date: October 2013
• Source: Kyorin University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Japan: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Evaluation of clinical characteristics and surgical outcome for macular detachment associated with peripapillary intrachoroidal cavitation with or without pathologic myopia.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 69
• Est. completion date: September 2013
• Est. primary completion date: March 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 10 Years to 95 Years

Eligibility

Inclusion Criteria:

• Eyes with macular detachment or macular retinoschisis

Exclusion Criteria:

• Optic pit maculopathy, vitreomacular traction syndrome

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Intrachoroidal Cavitation
• Macular Detachment
• Macular Retinoschisis
• Retinoschisis

Intervention

Other:
• Vitrectomy

Locations

Country	Name	City	State
Japan	Kyorin Eye Center	Mitaka	Tokyo

Sponsors (1)

Lead Sponsor	Collaborator
Kyorin University

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual acuity	The numbers of the patients with visual recovery after surgical intervention	one year	No
Secondary	Optical coherence tomography	Anatomical improvement detected with optical coherence tomography after surgical intervention	one year	No