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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00804869
Other study ID # APEC-037
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date October 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
Health authority
Study type Observational

Clinical Trial Summary

Ultrasonography has become a critical ancillary test in the clinical practice of ophthalmology. It is commonly used as a standardized method for assessing intraocular biometry. The PalmScan ultrasonography (PsU) is a portable A-scan device that uses the same principles as the standard A-scan. The aim of the study is to compare the reliability of their measurements, in order to use them indistinctively.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 90 Years
Eligibility Inclusion Criteria: - Patients with indication for a standard A-mode ultrasound Exclusion Criteria: - No superficial anormalities. - Patients with external injuries. - Intraocular silicon oil. - Retinal detachment - Significant ocular pathologies.

Study Design


Intervention

Device:
PalmScan A2000 ultrasonography system (Micro Medical Devices, Calabasas, CA)
PalmScan biometric measurements
Standard A-mode ultrasound (Eye Cubed™, Ellex, Adelaide, Australia).
A-mode biometric measurements group

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 axial length (AL). during examination
Primary Anterior Chamber Deep (ACD) during examination
Primary Lens Thickness (LT) during examination