Role of oral lactoferrin in post refractive surgery dry eye.
Phase 3
- Conditions
- Health Condition 1: H521- Myopia
- Registration Number
- CTRI/2024/05/067780
- Lead Sponsor
- Dr R P Centre for Ophthalmic Sciences AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients undergoing refractive surgery.
2.Willingness to sign written informed consent and
follow up.
Exclusion Criteria
1.Patients with a history of ocular surgery other
than refractive surgery.
2.Pregnancy and feeding mothers.
3.Lactose intolerance or cow milk allergy.
4.Patients not willing for participate and follow
ups.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Prevalence of post refractive surgery dry eye comes to 10% from 35% at 6 month post surgeryTimepoint: Dry eye work up will be done at baseline, before refractive surgery then 1 week, 1 month, 3 month and 6 month post surgery
- Secondary Outcome Measures
Name Time Method Bioavailability of lactoferrin in tear filmTimepoint: Tear samples will be collected at baseline, before surgery then 1 month, 3 month and 6 month post refractive surgery