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
- 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
CATARACT EYES WITH NO COMORBIDITIES ASTIGMATISM OF -0.75D TO -2D UNILATERAL EYE.
CORNEAL ECTATIC CONDITIONS CORNEAL SCARS PTERYGIUM POST REFRACTIVE SURGERY GLAUCOMA RETINAL PATHOLOGIES.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO EVALUATE THE EFFICACY SAFETY AND PREDICTABILITY OF ARCUATE INCISIONS TO CORRECT CORNEAL ASTIGMATISM CREATED BY THE LENSAR FEMTOSECOND LASER DEVICE PREOP , POSTOP-1DAY,3MONTHS , 12 MONTHS
- Secondary Outcome Measures
Name Time Method TO EVALUATE REGRESSION OF ASTIGMATISM IN THE NEXT 12 MONTHS FOLLOW UP PERIOD PREOP , POSTOP-1DAY,3MONTHS , 12 MONTHS
Trial Locations
- Locations (1)
Nethradhama Superspeciality Eye Hospital
🇮🇳Bangalore, KARNATAKA, India
Nethradhama Superspeciality Eye Hospital🇮🇳Bangalore, KARNATAKA, IndiaDR SHEETAL BRARPrincipal investigator9591002092brar_sheetal@yahoo.co.in
