Effect of Selective Laser Trabeculoplasty Versus Travoprost on Circardian Intraocular Pressure

Intraocular Pressure Clinical Trial

Official title:

A Prospective, Randomized Study Comparing the Effects of Selective Laser Trabeculoplasty and Travoprost on the Circadian Intraocular Pressure Variation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02105311
• Other study ID #: EC57-020-02-1
• Status: Completed
• Phase: Phase 4
• First received: March 28, 2014
• Last updated: August 4, 2016
• Start date: March 2014
• Est. completion date: February 2016

Study information

• Verified date: August 2016
• Source: Prince of Songkla University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Thailand: Research Institute for Health Sciences
• Study type: Interventional

Clinical Trial Summary

The investigators conduct this study to access the effect of selective laser trabeculoplasty on 24-hour circadian tension curves of patients with open-angle glaucoma, normal tension glaucoma and ocular hypertension. This treatment effect is compared with that of the prostaglandin analogue, travoprost.

Description:

Selective laser trabeculoplasty is an effective treatment for lowering intraocular pressure in patients with open-angle glaucoma. Clinical evaluations of its effectiveness in individual patients usually are derived from baseline and post-laser measurements of intraocular pressure during office hours in the sitting position. Only a few studies have examined the efficacy of laser trabeculoplasty beyond office hours. Although the 24-hour effect of laser trabeculoplasty has been studied ,the study was conducted before the use of these new and more potent intraocular pressure lowering drugs. So it doesn't have any study to determine the effect of selective laser trabeculoplasty and travoprost to reduce the diurnal and nocturnal variation of Iintraocular pressure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: February 2016
• Est. primary completion date: February 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age > 18 year-old

• Patients who were diagnosed as primary open-angle glaucoma, normal tension glaucoma, and ocular hypertension either newly diagnosed or currently on medical therapy.

• Agree to participate in the study, accept to be randomized to receive treatment, and willing to sign an informed consent

Exclusion Criteria:

Related to the severity of disease and visual acuity status

• Advance glaucoma in the study eye

• Have a very high intraocular pressure that need immediate treatment to prevent retinal vein occlusion (intraocular pressure >30 mmHg)

• Currently on maximal tolerated medical treatment and unable to control intraocular pressure

• Currently on oral carbonic anhydrase inhibitor for intraocular pressure control

• Single eye, the other eye blind from any cause

Related to surgical procedures

• Prior laser trabeculoplasty

• Prior glaucoma surgery

• Prior retinal surgery

• Underwent less than 3-month cataract extraction

• Potential need for other ocular surgery within the 2-3-month follow-up period since enrollment Related to underlying and ocular history

• History of diabetic retinopathy staged as severe non-proliferative or worse

• Narrow iridocorneal angle

• Ocular condition precluding visualization of trabecular meshwork

• Recently have ocular inflammation of any cause

• Previous history of ocular trauma

• Pregnant or breast-feeding women Related to the difficulty of having reliable measurements

• History of refractive surgery or any keratoplastic procedure

• Corneal opacities or diseases making no suitable tonometry

• Subjects with having poor or eccentric fixation or nystagmus

• Excessive eye squeezing

• Unable to lay down for measuring intraocular pressure in supine position during the night time

• Unable to have intraocular pressure checked every 2-hour such as have complicated underlying diseases or having sleep deprivation Related to allergy

• Known allergy to topical anesthesia

• Known allergy to fluorescein solution

• Known allergy to travoprost Related to compliance

• Impairment preventing adequate understanding to sign an informed consent

• Subject has demonstrated potential for non-compliance with the study protocol

• Unwilling to be randomized to receive treatment

• Unwilling to be washed out from currently treated drug(s).

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Intraocular Pressure

Intervention

Device:
• Selective laser trabeculoplasty
Selective laser trabeculoplasty platform The Lumenis Selecta® Duet™ (Lumenis Ltd., Yokneam, Israel)

Drug:
• Travoprost
Travoprost benzalkonium-free ophthalmic solution (40 microgram/ml) (Alcon Laboratories, Inc., Fort Worth, TX, USA)

Locations

Country	Name	City	State
Thailand	Songklanagarind Hospital	Hatyai	Songkhla

Sponsors (1)

Lead Sponsor	Collaborator
Prince of Songkla University

Country where clinical trial is conducted

Thailand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of circadian intraocular pressure	intraocular pressure values measured during daytime and nighttime, compare between selective laser trabeculoplasty and travoprost (include pre- and post-treatment intraocular pressure values)	Six weeks after recieving treatment	No
Secondary	Position related intraocular pressure	Intraocular pressure different when measuring in the sitting and supine position (include pre- and post-treatment intraocular pressure values	Six weeks after the treatments	No
Secondary	Ocular surface disease	Using the glaucoma symptom scale-10 (GSS-10) and ocular surface disease questionnaire for evaluation	Six weeks after the treatments	Yes