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Active Not RecruitingNCT06913478

Evaluation Of Effect of Axial Length on Cup-To-Disc Ratio Among Non- Glaucomatous Hypertensive Patients

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
94 (actual)
Sponsor
Superior University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This observational cross-sectional study aims to compare the effect of axial length on the cup-to-disc ratio in non-glaucomatous hypertensive patients. Data will be collected from Khursheed Begum Eye Hospital and LRBT Hospital, with a sample size of 104 participants. A purposive sampling technique will be used.

Detailed description

Patients aged 18-70 years with systemic hypertension for at least one year and normal intraocular pressure will be included. Exclusion criteria include glaucoma, high myopia, hyperopia, ocular surgery, trauma, and optic nerve diseases. Axial length will be measured using optical biometry or A-scan ultrasonography, while the cup-to-disc ratio will be assessed through fundus examination using a slit lamp biomicroscope with a +90D lens or optical coherence tomography (OCT). Data will be meticulously documented, including patient demographics and medical history. The study will be completed within six months after approval, ensuring accurate and standardized measurements for reliable results.

Conditions

Timeline

Start date
2025-03-20
Primary completion
2025-06-20
Completion
2026-02-20
First posted
2025-04-06
Last updated
2025-04-06

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06913478. Inclusion in this directory is not an endorsement.

Evaluation Of Effect of Axial Length on Cup-To-Disc Ratio Among Non- Glaucomatous Hypertensive Patients (NCT06913478) · Clinical Trials Directory