Clinical trial · Interventional
To Compare the Clinical Outcomes of FemtoLASIK and ICL Implantation in Treating Moderate Myopia Focusing on Refractive Stability, Contrast Sensitivity and High Order Aberrations.
Comparing Visual Outcomes After FemtoLasik and Implantable Collamer Lens in Treatment of Myopia
NCT07291986CI-TRIAL-00099249completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Compare the clinical outcomes of FemtoLASIK and ICL implantation in treating moderate myopia.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Myopia, Moderate | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| FemtoLASIK | Procedure | — | UNRESOLVED |
| ICL implantation | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Simple Myopic Patients
- description
- Patients with simple myopia undergoing FemtoLASIK or ICL surgeries
- interventionNames
- Procedure: FemtoLASIK
- Procedure: ICL implantation
- type
- ACTIVE_COMPARATOR
- label
- Compound Myopic Patients
- description
- Patients with compound myopia undergoing FemtoLASIK or ICL surgeries
- interventionNames
- Procedure: FemtoLASIK
- Procedure: ICL implantation
Primary outcomes (3)
- measure
- Refractive Stability (%)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
- Maximum age
- 40 Years
Show eligibility criteria text
Inclusion Criteria: Group I - FemtoLASIK subgroup: * Age range: 21-40 years. * Stable myopia for at least one year (refractive change ≤ 0.50 D). * Spherical equivalent between -4.00 D and -8.00 D. * Corneal thickness ≥ 500 μm, residual stromal bed \> 300 μm and percentage of tissue altered \< 39%. * No evidence of keratoconus or ectatic changes on corneal topography/tomography. * Mesopic pupil diameter ≤ 6.5 mm. * Absence of ocular surface disease or significant dry eye symptoms. * No history of prior ocular surgery or trauma. Group II - ICL subgroup: * Age range: 21-40 years. * Stable myopia (with or without astigmatism) for ≥1 year. * Spherical equivalent between -4.00 D and -8.00 D. * Anterior chamber depth ≥ 2.8 mm from endothelium. * Endothelial cell density ≥ 2500 cells/mm². * White-to-white and sulcus-to-sulcus diameters suitable for ICL sizing. * Clear crystalline lens with no signs of early cataract. * No history of intraocular surgery, uveitis, or glaucoma. Exclusion Criteria: Patients with mild myopia (\<-4D) or high myopia (\>- 8D) or hyperopia. * Patients with media opacity. * Patients with associated ocular pathology. * Patients with corneal topography not fitting to either treatment modalities.
References
Publications (0)
Data not yet available
No reference posted for this study.