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Clinical Trials/CTRI/2017/08/009277
CTRI/2017/08/009277
Completed
Phase 4

A COMPARATIVE STUDY OF CENTRAL CORNEAL THICKNESS MEASURED BY OPTICAL COHERENCE TOMOGRAPHY AMONG PATIENTS OF PRIMARY OPEN ANGLE GLAUCOMA, NORMAL-TENSION GLAUCOMA AND OCULAR HYPERTENSION â?? CROSS SECTIONAL OBSERVATIONAL STUDY

Sir T Hospital Bhavnagar0 sites61 target enrollmentTBD
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ConditionsHealth Condition 1: null- Glaucoma

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: null- Glaucoma
Sponsor
Sir T Hospital Bhavnagar
Enrollment
61
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
January 30, 2018
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
Sir T Hospital Bhavnagar

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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