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Phacoemulsification Versus Phacoemulsification With Micro-bypass Stent

Primary Purpose

Primary Angle-Closure Glaucoma, Primary Angle Closure Without Glaucoma Damage

Status
Completed
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
iStent implantation
Sponsored by
Khoo Teck Puat Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Angle-Closure Glaucoma focused on measuring istent, primary angle closure

Eligibility Criteria

21 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • able to provide informed consent
  • Previous diagnosis of Primary Angle Closure or Primary Angle Closure Glaucoma
  • Intraocular Pressure above 21mmHg at 3 separate visits
  • On 1 or more hypotensive medications
  • Pre-operative visual acuity of no better than 6/12

Exclusion Criteria:

  • Other glaucoma diagnosis: Primary Open Angle Glaucoma, secondary glaucoma
  • Peripheral Anterior Synechiae in the nasal and inferior quadrant
  • Cloudy cornea affecting view for iStent implantation
  • Previous glaucoma surgery
  • History of Ocular trauma
  • Ocular surface disease
  • Pre-proliferative or proliferative diabetic retinopathy
  • Age related macular degeneration with macular scar or macular atrophy

Sites / Locations

  • Khoo Teck Puat Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

phacoemulsification alone

phacoemulsification and iStent

Arm Description

routine phacoemulsification cataract surgery with intraocular lens implantation

phacoemulsification cataract surgery with intraocular lens implantation combined with iStent implantation

Outcomes

Primary Outcome Measures

Change in Intraocular Pressure Between Baseline and 1 Year
change in mean unmedicated intraocular pressure between baseline and 1 year

Secondary Outcome Measures

Change in Glaucoma Medications
change in number of topical glaucoma medications at 1 year post operation

Full Information

First Posted
August 23, 2018
Last Updated
October 3, 2018
Sponsor
Khoo Teck Puat Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03647033
Brief Title
Phacoemulsification Versus Phacoemulsification With Micro-bypass Stent
Official Title
Phacoemulsification Versus Phacoemulsification With Micro-bypass Stent Implantation in Primary Angle Closure and Primary Angle Closure Glaucoma: Randomized Double-masked Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
October 14, 2015 (Actual)
Primary Completion Date
August 12, 2016 (Actual)
Study Completion Date
August 12, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Khoo Teck Puat Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Assessing the safety and efficacy of a micro-bypass stent in combination with cataract surgery in subjects with primary angle closure. Subjects are randomized into two arms: phacoemulsification cataract surgery alone versus phacoemulsification cataract surgery combined with the micro-bypass stent implantation. Post surgery intraocular eye pressure will be recorded to assess the efficacy of both arms.
Detailed Description
Aim: To assess the safety and efficacy of the iStent trabecular micro-bypass stent (Glaukos Corporation, Laguna Hills, CA) in combination with cataract surgery in subjects with primary angle closure and mild to moderate primary angle closure glaucoma Method: Prospective, randomised controlled trial, blinded to patient and intra-ocular pressure measuring staff. 32 patients, 1:1 ratio, in 2 arms of phacoemulsification alone compared to phacoemulsification with iStent. Hypothesis: Phacoemulsification with micro-bypass stent has a better intraocular pressure (IOP) lowering effect compared to phacoemulsification alone in primary angle closure and primary angle closure glaucoma at 1 year after surgery. Importance: Primary angle closure and primary angle closure glaucoma are conventionally treated with eye drops that lower the intraocular pressure (IOP). Phacoemulsification/lens extraction can often help lower the eye pressure by widening the drainage angle and via ultrasound mechanisms, however, in some cases the IOP is not lowered, or even can cause the IOP to be higher. The iStent implant can be used together with phacoemulsification to lower the IOP and in Primary open angle glaucoma, it gives an additional 20% IOP reduction. It is unclear what effect the iStent has in primary angle closure or primary angle closure glaucoma as it has never been studied. It is important because primary angle closure glaucoma is much more common in the Singaporean Chinese population and the iStent can potentially be used to control the IOP instead of conventional eye drops and glaucoma surgery which have their own potential adverse effects. Potential Benefits: iStent with phacoemulsification may control the IOP better than phacoemulsification alone, reduce the need for IOP lowering medication after surgery, and prevent the need for glaucoma surgery in the future. Potential Risks: The iStent has risks of IOP spikes, bleeding in the anterior chamber and iStent dislocation.Phacoemulsification has the risks of: infection, bleeding, reduced vision, inflammation, posterior capsular rupture, vitreous loss, retinal detachment, endophthalmitis, suprachoroidal haemorrhage and Intraocular Lens dislocation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Angle-Closure Glaucoma, Primary Angle Closure Without Glaucoma Damage
Keywords
istent, primary angle closure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Single centre, randomised prospective trial, the patient and the intraocular pressure (IOP)checking staff will be blinded. Randomised by random envelope shuffle technique. 1:1 ratio allocation 2 arms: phacoemulsification alone and phacoemulsification and iStent. 16 patients in each arm, 32 patients in total. The post-operative management is the same for both arms After operation the patient will be followed up at day 1, week 1, week 2, months 1, 3, 6 and 12. At each visit the patient will have the following tests: Tonometry (IOP check) - Not to be taken by the operating surgeon, to be taken by 2 people, one IOP checker and one reader.
Masking
ParticipantOutcomes Assessor
Masking Description
Shuffled envelope system. Patient will be blinded to the procedure. The intraocular pressure (IOP) measure and reader will be blinded to the procedure. There will be no planned breaking of randomization. Unplanned breaking will happen if any envelopes are damaged or lost. Unmasking will take place after 1 year post operation by the study team to inform the patient of the procedure.
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
phacoemulsification alone
Arm Type
No Intervention
Arm Description
routine phacoemulsification cataract surgery with intraocular lens implantation
Arm Title
phacoemulsification and iStent
Arm Type
Experimental
Arm Description
phacoemulsification cataract surgery with intraocular lens implantation combined with iStent implantation
Intervention Type
Device
Intervention Name(s)
iStent implantation
Intervention Description
The iStent is a FDA and Health Sciences Authority (HSA) approved micro-bypass stent device that bypasses the trabecular meshwork (filtration membrane of the aqueous fluid exit pathway) and reroutes aqueous from the anterior chamber directly into canal of Schlemm and out of the eye. It lowers the intraocular pressure (IOP) by increasing the outflow of fluid from the eye from the micro-bypass. In angle closure, the lens has to be removed to create enough space for the iStent to be inserted.
Primary Outcome Measure Information:
Title
Change in Intraocular Pressure Between Baseline and 1 Year
Description
change in mean unmedicated intraocular pressure between baseline and 1 year
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Change in Glaucoma Medications
Description
change in number of topical glaucoma medications at 1 year post operation
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: able to provide informed consent Previous diagnosis of Primary Angle Closure or Primary Angle Closure Glaucoma Intraocular Pressure above 21mmHg at 3 separate visits On 1 or more hypotensive medications Pre-operative visual acuity of no better than 6/12 Exclusion Criteria: Other glaucoma diagnosis: Primary Open Angle Glaucoma, secondary glaucoma Peripheral Anterior Synechiae in the nasal and inferior quadrant Cloudy cornea affecting view for iStent implantation Previous glaucoma surgery History of Ocular trauma Ocular surface disease Pre-proliferative or proliferative diabetic retinopathy Age related macular degeneration with macular scar or macular atrophy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philemon Huang, MMed, FAMS
Organizational Affiliation
National Healthcare Group, Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Khoo Teck Puat Hospital
City
Singapore
ZIP/Postal Code
768828
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22814041
Citation
Craven ER, Katz LJ, Wells JM, Giamporcaro JE; iStent Study Group. Cataract surgery with trabecular micro-bypass stent implantation in patients with mild-to-moderate open-angle glaucoma and cataract: two-year follow-up. J Cataract Refract Surg. 2012 Aug;38(8):1339-45. doi: 10.1016/j.jcrs.2012.03.025.
Results Reference
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PubMed Identifier
20202537
Citation
Fea AM. Phacoemulsification versus phacoemulsification with micro-bypass stent implantation in primary open-angle glaucoma: randomized double-masked clinical trial. J Cataract Refract Surg. 2010 Mar;36(3):407-12. doi: 10.1016/j.jcrs.2009.10.031.
Results Reference
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PubMed Identifier
26147908
Citation
Malvankar-Mehta MS, Iordanous Y, Chen YN, Wang WW, Patel SS, Costella J, Hutnik CM. iStent with Phacoemulsification versus Phacoemulsification Alone for Patients with Glaucoma and Cataract: A Meta-Analysis. PLoS One. 2015 Jul 6;10(7):e0131770. doi: 10.1371/journal.pone.0131770. eCollection 2015.
Results Reference
background
PubMed Identifier
20828829
Citation
Samuelson TW, Katz LJ, Wells JM, Duh YJ, Giamporcaro JE; US iStent Study Group. Randomized evaluation of the trabecular micro-bypass stent with phacoemulsification in patients with glaucoma and cataract. Ophthalmology. 2011 Mar;118(3):459-67. doi: 10.1016/j.ophtha.2010.07.007. Epub 2010 Sep 15.
Results Reference
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Phacoemulsification Versus Phacoemulsification With Micro-bypass Stent

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