Refractive Surgery
Conditions
Keywords
Topography guided ablation, Astigmatism, LASIK
Brief summary
Background and Rationale: LASIK has been among the highest satisfaction rates of surgical procedures, ranging from 82%-98%. Different ablation profiles have been developed over the years. The purpose of this study is to validate this novel measurement by comparing the visual outcomes when the TMR is used in myopic astigmatic LASIK to using the standard manifest refraction or the Topolyzer measurements alone. Objectives : To evaluate the safety, efficacy and predictability of topography-guided myopic LASIK with three different refraction treatment strategies.
Detailed description
Candidates for refractive surgery above 18 years with myopic astigmatism and no previous ocular surgery. Sample size 60 eyes. surgery: * 60 eyes of myopic topography-guided LASIK procedures with the same refractive platform (FS200 femtosecond to create a flap between90: 110 μm with diameter 8:9 mm and EX500 excimer lasers) will be randomized for treatment as follows: * Group A: 20 eyes will be treated using Contoura vision with the standard manifest refraction. * Group B: 20 eyes will be treated with Contoura vision using the topographic astigmatic power and axis and without change in the spherical power (using the same spherical power as the manifest refraction). * Group C \[TMR\]: 20 eyes will be treated with Contoura vision using the topographic astigmatic power and axis and modifying the spherical power to obtain the same spherical equivalent as the manifest refraction. This is done by subtracting half of the difference between topographic astigmatic power and the manifest astigmatic power from the spherical power (topography-modified treatment refraction). * The standard postoperative treatment is combined steroids and antibiotics eye drops 5 times daily for one week ,then three times daily for three days and lubricant eye drops 5 times daily for six months. Postoperatively, the patients will be examined at 1 week, 1 month and 3 months. All postoperative follow-up visits included measurement of UDVA, CDVA (if indicated) and refraction, besides full ophthalmological examination and performing pentacam and topolyzer after 3 months
Interventions
PROCEDUREtopography guided ablation
using the data obtained from the topolyzer for correction of refractive errors specially astigmatism we use 3 different treatment protocols
PROCEDUREmanifest refraction
using for ablation the exact manifest refraction
PROCEDUREfull topography modified refraction
full topography modified refraction means changing both sphere and cylinder power in the ablation profile
PROCEDUREpartial topography modified refraction
partial topography modified refraction means changing only cylinder power and axis in the ablation profile
Sponsors
Cairo University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Intervention model description
A prospective, randomized and comparative interventional study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Stable refractive error: Myopic astigmatism ≥ -1.5 D * Valid Topolyzer maps (at least four out of eight right maps with green analyzed area and the registration box is green).
Exclusion criteria
1. Estimated postoperative residual stromal bed thickness of less than 300µm. 2. Glaucomatous patients. 3. Patients with keratoconus. 4. Patients with pervious refractive surgery. 5. History of previous ocular trauma or surgery. 6. History of recent herpetic ulcer or viral keratitis. 7. Basement membrane disease, history of recurrent corneal erosions. 8. Sicca syndrome, dry eye.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| post operative residual astigmatism | 3 months | measuring the post operative residual astigmatism and comparison between the 3 group to reach to the most accurate protocol. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| measurement of the postoperative unaided visual acuity | 3 months | measurement of the postoperative unaided visual acuity and comparison between the 3 group to reach to the most accurate protocol. |
Countries
Egypt
Outcome results
None listed