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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02843594
Other study ID # LEEP103
Secondary ID
Status Recruiting
Phase Phase 4
First received July 20, 2016
Last updated August 22, 2016
Start date August 2016
Est. completion date September 2018

Study information

Verified date August 2016
Source Iantech, Inc
Contact Jennifer Gaines
Phone +1 (415) 295-4770
Email admin@iantechmed.com
Is FDA regulated No
Health authority Panama: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to evaluate the clinical outcomes of different cataract surgical techniques for lens fragmentation in subjects undergoing routine cataract surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date September 2018
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Able to understand study requirements, willing to follow study instructions and willing to return for required study follow-up visits as confirmed by provision of written informed consent.

2. Subjects with a visually significant cataract scheduled to undergo cataract surgery

3. Subjects > 18 years of age

4. BCVA at baseline not better than 20/40

5. Grade 1+ cataracts

Exclusion Criteria:

1. Subjects not able to complete the informed consent form

2. Subjects < 18 years of age

3. Polar cataracts

4. Zonular instability

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
LEEP intervention
Low Energy Endosafe Phaco (LEEP) with micro-interventional lens fragmentation
Standard Phaco Control


Locations

Country Name City State
Panama Clinica de Ojos Panama City Panama

Sponsors (1)

Lead Sponsor Collaborator
Iantech, Inc

Country where clinical trial is conducted

Panama, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cumulative Dispersed Phaco energy Total phaco power and energy used as recorded by the phaco machine Intraoperative No
Secondary Endothelial cell loss Change from baseline endothelial cell density as measured by specular microscopy 1 month Yes
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