Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03266406
Other study ID # effect of hyaluronidase on IOP
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 28, 2017
Last updated August 28, 2017
Start date September 2017
Est. completion date October 2018

Study information

Verified date August 2017
Source Assiut University
Contact Eman Yassin
Phone 00201004686028
Email emanyassin08@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate effect of retrobulbar local anaesthesia after addition of hyaluronidase on IOP during cataract surgery


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date October 2018
Est. primary completion date September 2018
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

- 1-Patients above the age of 50 years. 2-Patients with age related cataract. 3-Normal IOP.

Exclusion Criteria:

- 1History of trauma. 2-Patients with glaucoma. 3-Previous ocular surgery. 4-Patients with other ocular pathology. 5-Uncontrolled diabetes or hypertension. 6-hypersensitivity to lignocaine. 7-Uncooperative or epileptic patients.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Hyaluronidase
4ml of retrobulbar LA with addition of 15IU/ml hyaluronidase to 2% lidocaine

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary reduction in IOP reduction of complications of high IOP during surgery within 10minutes