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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02638025
Other study ID # HMCH20151216
Secondary ID
Status Completed
Phase N/A
First received December 16, 2015
Last updated December 20, 2015
Start date January 2010
Est. completion date July 2015

Study information

Verified date December 2015
Source Huizhou Municipal Central Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

This study use anterior segment spectral-domain optical coherence tomography (SD-OCT) to exam patients with closed globe injury, and compared with slit lamp examination. The results showed that OCT can identify features of closed globe injury that were otherwise not visible on slit lamp biomicroscopy.


Description:

The anterior segment architecture changes of closed globe injury patients include corneal damage, hyphema, angle recession and lens dislocation, which can be showed with OCT. OCT was superior to slit lamp biomicroscopy examination in detecting anterior segment architecture changes, especially in the presence of media opacities.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date July 2015
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- patients with closed globe injury were recruited; had hyphema at least 1/3 of anterior chamber volume

Exclusion Criteria:

- can not cooperate with examination

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
OCT
Anterior Segment Spectral-domain Optical Coherence Tomography

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Huizhou Municipal Central Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary anterior segment spectral-domain optical coherence tomography (SD-OCT) findings in patients with closed globe injury within 24 hours after patients were admitted No
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