Trientine Hydrochloride for the Prevention of Macular Edema Associated With Pan-retinal Photocoagulation for Severe Non-proliferative and Proliferative Diabetic Retinopathy

NCT ID: NCT01213888

Last Updated: 2013-05-03

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-11-30
• Study Completion Date: 2013-04-30

Brief Summary

To evaluate the effects of Trientine Hydrochloride in prevention of post-laser (pan-retinal photocoagulation) macular edema in the eyes for subjects with diabetic retinopathy. Trientine hydrochloride can limit secondary inflammatory damage to retinal vessels following the administration of pan-retinal photocoagulation therapy for severe non-proliferative diabetic retinopathy or retinal neovascularization due to diabetic retinopathy, resulting in less macular edema and improved visual outcomes.

Detailed Description

Individuals with new-onset severe non-proliferative diabetic retinopathy or retinal neovascularization who present to the retinal service of the UBC/VGH Eye Care Centre will be offered participation in this study. Subject inclusion criteria will parallel those of the DRS (Diabetic Retinopathy Study) and ETDRS (Early Treatment of Diabetic Retinopathy Study). One PRP session will consist of between 800 to 1000 laser burns. Subjects with discomfort during laser (a known side-effect) will be treated with local anesthetics.

As noted, participating subjects will all receive PRP according to present standards of care; however, subjects will be randomized to either a 10-day course of oral Trientine at 1500mg administered for 7-days prior to and 3 days after the PRP sessions, or a placebo. Serum copper levels and urinary copper levels will be evaluated before and after Trientine administration to determine the amount of free copper present systemically at the time of PRP treatment.

Ocular outcomes will include visual acuity testing (ETDRS), fluorescein angiography and ocular coherence tomography (OCT). These studies will be used to evaluate retinal morphology and photoreceptor function pre and post laser. All these evaluations are considered part of the routine evaluation of diabetic retinopathy in subjects being treated with PRP.

Outcome measures will be assessed at day 2-post laser, week 1, and Day 28-30. Further clinical PRP treatment will be administered if necessary after Day 28-30 at the discretion of the patients' ophthalmologist.

The primary analysis will involve comparing the retinal thickness measurements between subjects undergoing PRP with and without Trientine use. Secondary analyses will involve evaluations of visual acuity and fluorescein angiography. As well, changes in visual acuity, angiographic leakage, and retinal thickness will be regressed against serum copper levels. Sample size calculations suggest 15 subjects per arm should be adequate to demonstrate a 40% reduction in retinal thickness with a power of 80% comparing subjects receiving Trientine to controls.

Subjects who are randomized to Trientine will receive 1500 mg Trientine PO daily for 10 days. Subjects, study-coordinators, and investigators will be masked to treatment group. The primary analysis will be a comparison of OCT thickness measurements.

This is a single centre study involving 30 subjects (15 cases and 15 controls). A 1:1 randomization will be employed (Trientine 1500 mg: Placebo). No normal subjects will be enrolled.

Conditions

Diabetic Retinopathy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Blinding Strategy: DOUBLE

Study Groups

Arm II

Group Type: EXPERIMENTAL

Trientine Hydrochloride

Intervention Type: DRUG

All participating subjects will all receive PRP (pan-retinal photocoagulation) according to present standards of care; however, subjects randomized the intervention group (trientine hydrochloride) will be on a 10-day course of oral Trientine at 1500mg administered for 7-days prior to and 3 days after the PRP sessions.

Arm I. Placebo + Pan-Retinal Photocoagulation

All participating subjects will all receive PRP (pan-retinal photocoagulation) according to present standards of care; however, subjects randomized the placebo group will be on a 10-day course of oral placebo capsules at 1500mg administered for 7-days prior to and 3 days after the PRP sessions.

Group Type: PLACEBO_COMPARATOR

Oral placebo capsules

Intervention Type: DRUG

All participating subjects will all receive PRP (pan-retinal photocoagulation) according to present standards of care; however, subjects randomized the placebo group will be on a 10-day course of oral placebo capsules at 1500mg administered for 7-days prior to and 3 days after the PRP sessions

Interventions

Trientine Hydrochloride

All participating subjects will all receive PRP (pan-retinal photocoagulation) according to present standards of care; however, subjects randomized the intervention group (trientine hydrochloride) will be on a 10-day course of oral Trientine at 1500mg administered for 7-days prior to and 3 days after the PRP sessions.

Intervention Type: DRUG

Oral placebo capsules

All participating subjects will all receive PRP (pan-retinal photocoagulation) according to present standards of care; however, subjects randomized the placebo group will be on a 10-day course of oral placebo capsules at 1500mg administered for 7-days prior to and 3 days after the PRP sessions

Intervention Type: DRUG

Other Intervention Names

Syprine

Eligibility Criteria

Inclusion Criteria

• Severe non-proliferative diabetic retinopathy or retinal neovascularization secondary to diabetic retinopathy meeting DRS criteria for PRP laser
• ETDRS (Early treatment of Diabetic Retinopathy Study) eye score of at least 34-73 letters (at 2 meters) (20/20 to 20/320) for study eye and 20/800 in non-study eye
• Clinical evidence of macular microantiopathy in the study eye (lipid or retinal thickness is acceptable)
• No other ocular disease that could be responsible for decreased vision, macular edema or could limit macular imaging

Exclusion Criteria

• Individuals with retinal neovascularization from causes other than diabetic retinopathy
• Any intraocular surgery within 2 months or Yag capsulotomy within 1 month in the study eye
• Prior retinal or vitreous surgery (including posterior segment vitrectomy or scleral buckling)
• Medical conditions requiring the use of mineral supplements (copper in particular)
• Individuals with anemia
• Individuals with mental or physical disabilities that prevent accurate vision testing
• History of treatment of PDR by PRP
• Active hepatitis, clinically significant liver disease or any evidence of renal failure.
• Stroke or myocardial infarction within preceding 6 months or ventricular tachycardia under treatment
• History of severe cardiac disease or unstable angina
• Subjects who are in an experimental therapy study or who have received experimental therapy within the last 12 weeks
• Subjects who are a poor medical risk because of other systemic diseases or active uncontrolled infections
• Women of childbearing potential not on 2 effective forms of birth control
• Women who are pregnant or plan to become pregnant
• Subjects with an allergy to fluorescein dye.

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of British Columbia

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Patrick Ma

Role: STUDY_DIRECTOR

University of British Columbia

Andrew Merkus

Role: STUDY_DIRECTOR

University of British Columbia

David Albiani

Role: STUDY_DIRECTOR

University of British Columbia

David Maberly

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Locations

Eye Care Centre - Vancouver Coastal Health

Vancouver, British Columbia, Canada

Countries

Canada

Other Identifiers

H08-01900

Identifier Type: -

Identifier Source: org_study_id