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Micropulse Transcleral Cyclophotocoagulation in the treatment of refractary glaucoma

Not Applicable
Conditions
Glaucoma, IOP.
Unspecified glaucoma
Registration Number
IRCT20170325033136N2
Lead Sponsor
Alexandra Preda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
100
Inclusion Criteria

Intraocular pressure higher than 21 mmhg
Age > 18
Signed informed consent

Exclusion Criteria

Uveitis
Ocular surgery in the last 3 months, prior to study enrolment.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
IOP decrease. Timepoint: 1 week, 1 month, 3 months,6 months, 1 year. Method of measurement: Goldman aplanotonometry.
Secondary Outcome Measures
NameTimeMethod
Pain endurance. Timepoint: 5 minutes after procedure. Method of measurement: VAS scale.;Number of eye drops after the procedure to control the IOP. Timepoint: 1 month, 6 months, 1 year. Method of measurement: Asking patient.
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