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TO EVALUATE THE SAFETY EFFICIENCY AND PREDICTABILITY OF THE INCISIONS CREATED ON THE CORNEA BY THE FEMTOSECOND LASER (LENSAR) ASSISTED CATARACT SURGERY TO CORRECT PREOPERATIVE CORNEAL ASTIGMATISM AT THE TIME OF CATARACT SURGERY

Not yet recruiting
Conditions
cataract
Registration Number
CTRI/2021/12/038418
Lead Sponsor
LENSAR
Brief Summary

Phacoemulsification is the gold standard for cataract surgery. With constant improvements and continuous upgradations, most of the modern phacoemulsification systems on the market have improved on safety and efficacy, leading to reduced surgical times and lower rates of intra-operative complications, translating into better postoperative outcomes and patient satisfaction. Surgical efficiency, however, may vary, depending upon the surgeon’s skills as well as the machine settings. A good clinical outcome depends on the combination of both.

In line with these advancements, a new femtosecond laser system “LENSAR†has been recently updated to correct the topographic pre-operative astigmatism by arcuate incisions. The system has a unique ability to mark the arcuate incision on the cornea with the inbuilt woodcock nomogram, the reference image can directly be transferred to the LENSAR from the Pentacam, or if old versions of Pentacam are used it can also be transferred through an external hard disk, the device also has a unique ability to auto correct the cyclorotation by iris identification software after the patient is in supine position to maximize the results.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

CATARACT EYES WITH NO COMORBIDITIES ASTIGMATISM OF -0.75D TO -2D UNILATERAL EYE.

Exclusion Criteria

CORNEAL ECTATIC CONDITIONS CORNEAL SCARS PTERYGIUM POST REFRACTIVE SURGERY GLAUCOMA RETINAL PATHOLOGIES.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
TO EVALUATE THE EFFICACY SAFETY AND PREDICTABILITY OF ARCUATE INCISIONS TO CORRECT CORNEAL ASTIGMATISM CREATED BY THE LENSAR FEMTOSECOND LASER DEVICEPREOP , POSTOP-1DAY,3MONTHS , 12 MONTHS
Secondary Outcome Measures
NameTimeMethod
TO EVALUATE REGRESSION OF ASTIGMATISM IN THE NEXT 12 MONTHS FOLLOW UP PERIODPREOP , POSTOP-1DAY,3MONTHS , 12 MONTHS

Trial Locations

Locations (1)

Nethradhama Superspeciality Eye Hospital

🇮🇳

Bangalore, KARNATAKA, India

Nethradhama Superspeciality Eye Hospital
🇮🇳Bangalore, KARNATAKA, India
DR SHEETAL BRAR
Principal investigator
9591002092
brar_sheetal@yahoo.co.in

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