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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01959802
Other study ID # Kyorineye014
Secondary ID Kyorineye014
Status Completed
Phase N/A
First received October 7, 2013
Last updated October 8, 2013
Start date April 2008
Est. completion date March 2012

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 recovery in foveal cone outer segment tips line defect and visual acuity after surgery for macular pseudohole


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date March 2012
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender Both
Age group 10 Years to 95 Years
Eligibility Inclusion Criteria:

- The patienst with macular pseudo hole

Exclusion Criteria:

- The patients with follow-up less than 6 months

Study Design

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


Related Conditions & MeSH terms


Intervention

Procedure:
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 Optical coherence tomography Anatomical recovery detected with optical coherence tomography after surgery one year No
Secondary Visual acuity Visual recovery after surgery one year No