Comparison of two gel like substances in terms of immediate rise in eye pressure after insertion of Visian Implantable Collamer Lens
- Conditions
- Health Condition 1: null- Healthy individuals undergoing ICL procedure in both eyes for correction of myopia and myopic astigmatism
- Registration Number
- CTRI/2014/05/004594
- Lead Sponsor
- ethradhama Eye Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 15
Patients of any gender, between the age group of 21 to 45 years, undergoing ICL surgery with
V4C (Centraflow) model for correction of Myopic refractive error including myopic astigmatism
(of any degree) will be included in the trial.
1.Adequate AC depth ( >2.8 mm from endothelium)
2.Healthy eyes besides myopic refractive error (of any degree amenable to correction with Visian ICL, Centraflow)
3. Stable refraction and corneal conditions within the last 12 months
4.Signed informed consent , willingness to participate in trial and subsequent follow ups
Glaucoma or IOP higher than 24mmHg
Posterior segment disorders (e.g. Retinal degenerations , macular pathology, optic nerve atrophy, hereditary retinal disorders)
Pseudophakia/ Aphakia
Corneal dystrophies / corneal degenerations /Corneal scarring
Irregular astigmatism (e.g. Keratoconus, Pallucid Marginal Degeneration etc)
Post corneal refractive surgery
Moderate to severe dry eye, Severe Contact lens induced ocular allergy
Congenital ocular anomalies â?? Aniridia/ Iris coloboma, microcornea, nanophthalmos
Amblyopia
Pseudoexfoliation Syndrome; Uveitis
Prior use of long term antiglaucoma or steroid medications
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method