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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03551808
Other study ID # 96316
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date January 1, 2017
Est. completion date June 1, 2018

Study information

Verified date April 2018
Source Shahid Beheshti University of Medical Sciences
Contact Hossien Mohammad Rabie, MD
Phone 9822591616
Email labbafi@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is determining the prophylactic effect of ketorolac tromethamine drop 0.5% eye drop on the functional and anatomical ocular characteristics of the diabetic patients after the phacoemulsification surgery. Cystoid macular edema (CME) is a ocular disease which the retinal thickness is increased by 30 % incidence at least or the visual acuity is decreased to 20/40 according to clinical definition. Ketorolac tromethamine is an non steroidal anti inflammatory medication which is used for treatment and Prophylactic for CME. Teh aim of this study is prophylactic effect of ketorolac tromethamine on choroidal and retinal thickness after Phacoemulsification in Diabetic Patients. In this randomized clinical trial, 102 eyes of 102 diabetic patients were included. All patients were undergone phacoemulsification surgery at Torfeh Eye Hospital between September 2015 and January 2017. To evaluate the prophylactic effect of ketorolac tromethamine topical eye drop, all cases were asked to apply it one day before the s:surgery in each 8 hours and continue it for 4 weeks after the surgery. Controls were not received placebo. All study population were examined using Snellen visual acuity chart, enhanced depth imaging optical coherence tomography (EDI-OCT). All patients were followed at 6, 12 and 24 weeks after the cataract surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 102
Est. completion date June 1, 2018
Est. primary completion date June 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 95 Years
Eligibility Inclusion Criteria:

- Diabetic patients (type II) with cataract

- Eligible patients at age range of 20 to 95 years old

Exclusion Criteria:

- Cases with a diabetic macular edema

- proliferative diabetic retinopathy

- history of intravitreal injection of bevacizumab and macular photocoagulation prior three months to the cataract surgery

- glaucoma

- refractive errors of more than ±6 diopters

- history of previous ocular surgery

- ocular pathological disorders

- history of systemic diseases

- history of medications which have a side effect on the retinal thickness

- patients with a follow up of less than 6 months

- individuals with any intraoperative complications will be excluded from this study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
using of Ketorolac Tromethamine Eye Drop
using of Ketorolac Tromethamine Eye Drop one day before the surgery in each 8 hours and continue it for 4 weeks after the surgery

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shahid Beheshti University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Best Corrected visual acuity Snellen visual acuity chart 24 weeks after the surgery
Secondary retinal and choroidal thickness enhanced depth imaging optical coherence tomography (EDI-OCT) 24 weeks after the surgery