Comparison of CCT (Central Corneal Thickness) in patients of Primary open angle glaucoma, Normal tension glaucoma, Ocular hypertension using OCT (Ocular Coherence Tomography)

Phase 4

Completed

• Conditions: Health Condition 1: null- Glaucoma

• Registration Number: CTRI/2017/08/009277
• Lead Sponsor: Sir T Hospital Bhavnagar

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2018-01-30
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 61

Inclusion Criteria

Patient having Primary Open Angle Glaucoma (POAG),

Patients having Normal-Tension Glaucoma (NTG),

Patients having Ocular Hypertension

Exclusion Criteria

Patients not giving written and informed consent;

Secondary Glaucoma ;

Angle closure Glaucoma;

Pre-existing retinopathy, visual field defects, Non- Gluacomatous optic atrophy ;

Any Corneal Pathology including Corneal opacities, Corneal scars, Corneal Oedema etc.;

H/O previous Intraocular surgery;

H/O previous Intraocular Laser treatment like Nd:YAG Laser PI;

Any Drugs or Treatment affecting Intraocular Pressure (IOP) like Steroid treatment, long term use of OC pills, oral beta-blockers ;

Any Drugs causing Corneal dryness which interfere with Central Corneal Thickness like antihistaminics and decongestants, NSAIDs, antidepressants like sertaline,etc. ;

Allergy to Mydriatic agents, Topical Anaesthetic drops, Fluorescein dye

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Central Corneal Thickness (CCT) of all the patients will be measured using Optical Coherence Tomography (OCT). <br/ ><br>Data will be collected and interpreted and analysed.Timepoint: 12 months

Secondary Outcome Measures

Name	Time	Method
ot applicableTimepoint: Not applicable