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Evaluation of dry eye following topical phacoemulsification surgery

Study on the Clinical Profile of Dry Eye following Topical Phacoemulsification - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/04/065964
Enrollment
40
Registered
2024-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: H590- Disorders of the eye following cataract surgery

Interventions

Intervention1: NIL: NIL

Sponsors

Acharya Vinoba Bhave Rural Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who will present with senile cataracts during the study period but also have no history of dry eye syndrome 2.Patients giving their consent for the study

Exclusion criteria

Exclusion criteria: 1.Patients with prior systemic diseases or syndromes associated with dry eye (example: diabetes mellitus, hypertension, deficiency of Vitamin A, diseases related to thyroid) 2.Patients who are on medications which have an additional side effect of causing ocular dryness (eg: diuretics, psychotropic’s, antihistaminic, antidepressants, decongestants, beta blocker drugs, diuretics, and aspirin)(6) 3.Patients who wear contact lens 4.patients with various adnexal disorders, anterior or posterior segment disorders that affect the stability and secretion of tears, patients on topical antiglaucoma medications that leads to ocular drying 5.conjunctivitis Which is chronic in nature 6.patients having small pupil or pupil which is difficult to dilate

Design outcomes

Primary

MeasureTime frame
dryness evaluation by tear film break up time, visual acuity, dryness evaluation by Schirmers test, dryness evaluation by tear meniscus height, ocular surface disease index questionnaire for evaluating symptoms of dryness.Timepoint: day 1, day 7 and day 30

Secondary

MeasureTime frame
1. dry eye 2. post operative inflammation 3. endophthalmitisTimepoint: day 30, day 60

Countries

India

Contacts

Public ContactDiksha Garg

Datta Meghe Institute of Higher Education and Research

drpktidake@gmail.com7887476011

Outcome results

None listed

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