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NCT05201677 Clinical Trial

Improved Operation of Low Intraocular Pressure in Phacoemulsification for Patients With High Myopia Complicated With Cataract

High Myopia Clinical Trial

Official title:
Improved Operation of Low Intraocular Pressure in Phacoemulsification for Patients With High Myopia Complicated With Cataract

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05201677
Other study ID # WDD-High myopia-Low IOP
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2021
Est. completion date June 1, 2022

Study information
Verified date January 2022
Source Wenzhou Medical University
Contact Dandan Wang
Phone 18258227706
Email wangdan4827716@yahoo.com.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Approximately 60 participants at Eye Hospital of Wenzhou Medical University during October,2021 to January 2022 will be enroll in the investigators' study. And dived them randomly into 2 groups:High myopia with axial length between 26 mm and 28 mm and High myopia with axial length more than 28 mm (30 eyes) .

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date June 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - The patients with high myopia and cataract who plan to receive cataract surgery in our hospital - Surgery without complications Exclusion Criteria: - Patients who had other ocular diseases or had undergone internal eye surgery - Patients with a history of myopic laser surgery - Previous history of eye trauma - Previous use of medications/eye drops that may alter IOP

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Supplement of perfusion fluid through the subiris suspensory ligament space from the lateral incision
After the capsule is filled with viscoelastic material, if the IOP is less than 10 mmHg, the investigators will supply the perfusion fluid through the subiris suspensory ligament space from the lateral incision.

Locations
Country Name City State
China Eye Hospital of Wenzhou Medical College Wenzhou Zhejiang

Sponsors (1)
Lead Sponsor Collaborator
Yune Zhao

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intraocular pressure Measurement of intraocular pressure during cataract surgery by iCare rebound tonometer two minutes
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