Time Study for Biometry Measurements With the Lenstar and IntraOcularLens (IOL) Master 500

• Sponsor: Haag Streit USA (Industry)
• Overall Status: Completed
• CT.gov ID: NCT01550939
• Collaborator: (none)
• Enrollment: 61
• Location: 1
• Arm: 1
• Duration (Months): 2
• Patients Per Site Per Month: 30.9

Study Details

Study Description

Brief Summary

The objectives of this study are to determine the time needed to complete a full set of measurements (Total Ophthalmic Exam, Subject Data Entry and Acquisition of the Measurement) by each test device, the Lenstar 900 Version i4 and IOL Master 500.

Condition or Disease	Intervention/Treatment	Phase
Pseudoaphakia	Device: Ophthalmic Biometer	Phase 4

Detailed Description

This is an open-label study randomized by sequence. Each eligible subject who signs a consent form and fulfills all Inclusion/Exclusion criteria will undergo ophthalmic measurements by the two test products:

1. Haag-Streit Lenstar Version i4

2. Zeiss IOL Master 500

The order of measurements for the IOL Master 500 and the Haag-Streit Lenstar Version i4 will he randomized. The two possible sequences will be balanced (approximately 22 eyes each: AB,BA). One eye of each subject will be measured. Time needed to complete testing will be measured utilizing a stop-watch. Total time needed to complete all measurements of the study eye using each of the test products to capture a complete ophthalmic exam with the devices standard operating settings set to automatic measurement and analysis will be calculated by the following start and stop points:

First Timed Measurement: Measurement Acquisition Start: When the technician starts to acquire tbe first measurement Stop: When the technician has completed all measurements

Second Timed Measurement: Subject Data Entry Start: When the technician starts to enter the subject data. Stop: When the technician has completed subject data entry.

Third Timed Measurement: Complete Ophthalmic Exam with each test product Start: When tbe subject is seated at the instrument, just prior to the technician entering any subject data into the test product.

Stop: Upon completion of all measurements using one of the test products, just prior to printing results.

Three trained technicians will operate tbe same study devices (Haag-Streit Lenstar Version i4 and IOL Master 500). Approximately equal number of subjects will be assigned to each technician.

Study Design

• Study Type: Interventional
• Actual Enrollment: 61 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Diagnostic
• Official Title: A Single-Center, Open-Label, Randomized Clinical Study Measuring Time Needed for Testing Between the Haag-Streit Lenstar 900 Version i4 and the Carl Zeiss IOL Master 500 Instruments
• Study Start Date: Jan 1, 2012
• Actual Primary Completion Date: Mar 1, 2012
• Actual Study Completion Date: Mar 1, 2012

Arms and Interventions

Arm	Intervention/Treatment
No Intervention: Time Comparison between the Lenstar and IOLMaster	Device: Ophthalmic Biometer; One complete biometry examination; Other Names: Haag-Streit Lenstar Zeiss IOL Master 500

Outcome Measures

Primary Outcome Measures

1. Time to complete a full examination [At Study Visit (study consists of 1 visit only)]

   Time to complete a full ophthalmic exam(as measured from the time of subject placement just prior to the technician completing data entry at the test product, to the beginning of data printing) for each, the IOL Master 500 and the Haag-Streit Lenstar Version i4.

Secondary Outcome Measures

1. Data Entry Time Measurement [At Study Visit (study consists of 1 visit only)]

   Additional Time Measurements - Data Entry from the IOL Master 500 and the Haag-Streit Lenstar Version i4.

2. Measurement Acquisition Time Measurement [At Study Visit (study consists of 1 visit only)]

   Additional Timed Measurements - Measurement Acquisition from the IOL Master 500 and the Haag-Streit Lenstar Version i4.

3. Adverse Events [Duration of study from signing informed consent to Study Visit (study consists of 1 visit only)]

   Any adverse events associated with the test products

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

Subjects wbo meet all of the following criteria are eligible to participate in tbe study:

1. Male or female l8 years of age or older on the date of Informed Consent.

2. At least one eye of each subject must be a phakic eye.

3. Subject must be able to fixate on a target.

4. Able to understand and willing to sign tbe informed consent.

Exclusion Criteria:

Subjects will be excluded from the study if the following applies:

1. History of corneal surgery.

2. Use of contact lenses during tbe ophthalmic exam or up to two hours prior to the exam.

3. Any ophthalmic condition preventing use of either of the instruments used in the study.

4. Any ophthalmic condition which might impair tbe validity of results from any of the instruments used in the study.

5. Any medical condition, which, in tbe Investigator's judgment, interferes with the subjects ability to comply with tbe protocol, compromises subject safety, or interferes with tbe interpretation of the study results.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Cincinnati Eye Institute	Cincinnati	Ohio	United States	45242

Sponsors and Collaborators

• Haag Streit USA

Investigators

• Principal Investigator: Michael E. Snyder, MD, Cincinnati Eye Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Haag Streit USA
• ClinicalTrials.gov Identifier: NCT01550939
• Other Study ID Numbers: HS1 Time Study 2
• First Posted: Mar 12, 2012
• Last Update Posted: Aug 1, 2012
• Last Verified: Jul 1, 2012

• Keywords provided by Haag Streit USA: Biometry of the Eye; Intraocular Lens Implantation; IOL
• Additional relevant MeSH terms: Cataract

Study Results

No Results Posted as of Aug 1, 2012