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Study to compare two different method of laser cataract surgery to avoid any glasses in future for distance vision.

Comparative analysis of intrastromal versus anterior penetrating astigmatic keratotomy incisions for correction of astigmatism in femtolaser assisted cataract surgery.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/07/006003
Enrollment
50
Registered
2015-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Healthy individuals with cataract and astigmatism.

Interventions

Intervention1: anterior penetrating astigmatic keratotomy: method to correct cylindrical power by laser which make cut at surface of cornea. Control Intervention1: intrastromal astigmatic keratotomy:

Sponsors

Nethradhama Superspeciality Eye Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • A patient with cataract for which phacoemulsification extraction and a posterior chamber IOL implantation has been planned • Male or female in good general health, 18 years of age or older at the time of the pre-operative examination • A patient has the visual potential of 20/25 or better in each eye after cataract removal and IOL implantation • A patient with preoperative corneal astigmatism of between 0.75D and 1.5D • A patient with no more than 1D difference in the amount of corneal astigmatism in each eye • A patient with clear ocular media other than cataract in each eye • A patient with normal OCT of the macula in each eye

Exclusion criteria

Exclusion criteria: • A patient with a known pathology that may affect visual acuity (as determined by the Investigator); particularly retinal changes that affect vision (macular degeneration, cystoid macular edema, proliferative diabetic retinopathy, etc.) in either eye • A patient with amblyopia or strabismus • A patient with capsule or zonular abnormalities that may affect postoperative centration or tilt of the lens (e.g. pseudoexfoliation syndrome) in either eye • A patient with visually significant Epithelial Basement Membrane Dystrophy on slit-lamp exam in either eye • A patient with evidence of Keratoconus or significant irregular astigmatism on pre-operative topography in either eye • A patient has a history of significant ocular trauma or prior ocular surgery in either eye • A patient that may or is expected to undergo surgical intervention and/or ocular laser treatment prior to or during the study period in either eye • A patient that had refractive surgery (LASIK, LASEK, RK, PRK, etc.) prior to cataract surgery in either eye • A patient that has been wearing PMMA lenses within 6 months, gas permeable lenses within one month, or extended-wear or daily soft contact lens within 7 days of their scheduled surgery • A patient that requires the use of systemic or ocular medications that may affect vision • A patient with any uncontrolled systemic disease. A potential patient in whom therapy for a systemic disease is not yet stabilized will not be considered for entry into the study • A patient currently participating or has participated within 30 days prior to thestart of this study in a drug or other investigational research study.

Design outcomes

Primary

MeasureTime frame
Residual astigmatism after surgery.Timepoint: Day 1, 15 and 3 month after surgery.

Secondary

MeasureTime frame
Change in aberrations and corneal topography.Timepoint: Day 1, 15 and 3 month after surgery.

Countries

India

Contacts

Public ContactSri Ganesh

Nethradhama Superspeciality eye hospital

drrahulp2012@gmail.com9731809663

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026