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To study and compare the effect of prednisolone acetate and nepafenac eyedrops in patients after surgery for cloudy lens (safed motiya)

A comparative evaluation of efficacy and safety of Prednisolone acetate and Nepafenac eye drops in post-operative cataract surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049131
Enrollment
40
Registered
2023-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: H269- Unspecified cataract

Interventions

Intervention1: Nepafenac eyedrops: Group B- Nepafenac (0.1%) eye drops three times a day for 3 weeks Intervention2: Nepafenac eyedrops: Group B- Nepafenac (0.1%) eye drops three times a day for 3 week

Sponsors

Pt B D Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients above 45 years of age with senile cataract undergoing phacoemulsification 2. Patients of either sex will be included 3. Patient willing to give written informed consent

Exclusion criteria

Exclusion criteria: 1. Patients with presenile cataract, glaucoma, uveitis, complicated cataract, subluxated cataract, traumatic cataract or posterior segment pathology 2. Patients sensitive to aspirin and other related NSAIDs 3. Use of systemic or topical steroids within 2 weeks of surgery 4. Use of systemic or topical NSAIDs within 7 days of surgery 5. Patient with uncontrolled diabetes 6. Any intraoperative complication

Design outcomes

Primary

MeasureTime frame
1. Change from baseline in Central corneal thickness post cataract surgery. 2. Resolution of anterior chamber reaction. 3. Improvement in visual acuity following cataract surgery.Timepoint: Patients will be evaluated at post-operative day 1, 1 week and 3 weeks. Any adverse drug reaction if occurs at any point in the study, has to be reported promptly and ADR monitoring to be done throughout the study.

Secondary

MeasureTime frame
1. Change from baseline Intraocular pressure following cataract surgery. 2. Improvement in patient comfort post cataract surgery.Timepoint: Patients will be evaluated at post-operative day 1, 1 week and 3 weeks.

Countries

India

Contacts

Public ContactDr Sumit Kumar

Pt. B D Sharma PGIMS Rohtak

drjarnailuhsr@gmail.com7206142252

Outcome results

None listed

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