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Steroids and/ or Non-steroidal Anti-inflammatory Drugs in the Postoperative Regime After Trabeculectomy. (SNAP)

Primary Purpose

Glaucoma

Status
Active
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Voltaren Ophtha 1 mg/ml, GSK
Monopex 1 mg/ml, Théa
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Glaucoma focused on measuring Trabeculectomy, NSAID, Steroid, Anti-Inflammatory Agents, Anti-Inflammatory Agents, Non-Steroidal, Eye Diseases

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with primary open-angle glaucoma (POAG), pseudoexfoliation syndrome (PEX), pigment dispersion syndrome (PDS) or ocular hypertension
  • >50 years
  • Women must be postmenopausal. Women are asked if they have menstruated within the preceding 12 months
  • Scheduled to undergo trabeculectomy surgery at the Department of Ophthalmology at Rigshospitalet-Glostrup, Denmark
  • Informed consent to participation and ability to comply with study procedures

Exclusion Criteria:

  • Known allergy to any of the contents of the pharmaceuticals (active and in-active ingredients) used in the study
  • Prior intraocular surgery, except from cataract surgery. If cataract surgery has been performed, it should at least be 6 months prior to surgery
  • Medical history of anterior segment dysgenesis, inflammatory/uveitic glaucoma, angle closure glaucoma, neovascular glaucoma and traumatic glaucoma
  • Steroid responders
  • Pregnancy
  • Fertile women, i.e. women who are not menopausal and women who breastfeed
  • Patients in systemic treatment with steroid or NSAID

Sites / Locations

  • Department of Ophthalmology

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Experimental

Arm Label

Topical, preservative-free NSAID

Topical, preservative-free steroid

Topical, preservative-free NSAID (Voltaren Ophtha 1 mg/ml, GSK

Arm Description

Topical medication are to be used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per week.

Topical medication are to be used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per week.

Topical medication are to be used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per wee

Outcomes

Primary Outcome Measures

Intraocular pressure (IOP)
Postoperative intraocular pressure (IOP) by applanation tonometry

Secondary Outcome Measures

Best corrected visual acuity
Postoperative best corrected visual acuity in logarithm to the minimal angle of resolution (logMAR)
Visual field
Postoperative changes in visual field by octopus autoperimetry. (MD)
Optical nerve damage
Optical nerve damage, assessed by measuring retinal nerve fiber layer (RNFL) by peripapillary optical coherence tomography (OCT)
Surgical success
The definition of surgical success criteria is dependent on the the severity of visual field defect (MD, mean deviation of visual sensitivity compared to those expected from the age-matched normative database) glaucoma diagnosis and achievement of target pressure without the use of medication (complete success) or with the use of glaucoma medication (qualified success) Ocular hypertension, target <25 mmHg MD < 6 dB, target < 21 mmHg MD 6 dB - 12 dB, target <18 mmHg MD > 12 dB, target < 15 mmHg

Full Information

First Posted
August 9, 2019
Last Updated
October 25, 2022
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT04054830
Brief Title
Steroids and/ or Non-steroidal Anti-inflammatory Drugs in the Postoperative Regime After Trabeculectomy.
Acronym
SNAP
Official Title
Steroids and/ or Non-steroidal Anti-inflammatory Drugs in the Postoperative Regime After Trabeculectomy. An Investigator-initiated Randomized Study (The SNAP Study)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 1, 2019 (Actual)
Primary Completion Date
June 15, 2022 (Actual)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

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

5. Study Description

Brief Summary
PURPOSE: Glaucoma is the leading cause of non-curable blindness globally. Patients with glaucoma will get a gradual narrowing of the visual fields caused by compression at the optic nerve head due to increased intraocular pressure. Thus the main preventive strategy is to reduce intraocular pressure, initially by eye drops and/or laser treatment but in some patients surgery is warranted. The surgical procedure (trabeculectomy) most widely performed worldwide creates a path from the anterior chamber to the subconjunctival space and thereby lowers the IOP by producing a more efficient drainage of the aqueous humour. Surgical success depends upon controlling post-operative inflammation to ensure a functional drainage. The purpose of this blinded, randomized study is to investigate which anti-inflammatory treatment provides better long-term control of intra-ocular pressure (IOP) following glaucoma surgery (trabeculectomy) by comparing topical NSAIDs to topical steroids. Additionally, we want to explore the mechanisms behind the pathophysiology of glaucoma by evaluating retinal and optic nerve head perfusion before and after IOP lowering surgery. The primary outcome is the intraocular pressure 12 months after surgery measured by applanation tonometry. MAIN HYPOTHESIS: NSAIDs and steroids are equally effective in assuring long-term filtering function and controlling IOP after trabeculectomy but may be associated with different risk profiles and bleb morphology Patients with lower post-operative IOP demonstrate less progression of visual field loss Trabeculectomy lowers IOP and provides better microcirculation in and oxygenation of inner retinal layers (i.e. ganglion cell layer) and the optic nerve head

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glaucoma
Keywords
Trabeculectomy, NSAID, Steroid, Anti-Inflammatory Agents, Anti-Inflammatory Agents, Non-Steroidal, Eye Diseases

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Topical, preservative-free NSAID
Arm Type
Experimental
Arm Description
Topical medication are to be used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per week.
Arm Title
Topical, preservative-free steroid
Arm Type
Active Comparator
Arm Description
Topical medication are to be used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per week.
Arm Title
Topical, preservative-free NSAID (Voltaren Ophtha 1 mg/ml, GSK
Arm Type
Experimental
Arm Description
Topical medication are to be used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per wee
Intervention Type
Drug
Intervention Name(s)
Voltaren Ophtha 1 mg/ml, GSK
Intervention Description
Voltaren Ophtha 1 mg/ml, eye drops used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per week.
Intervention Type
Drug
Intervention Name(s)
Monopex 1 mg/ml, Théa
Intervention Description
Monopex 1 mg/ml, eye drops used 6 times daily for the 2 first weeks, tapering to 4 drops per day for the next 4 weeks. Depending on the clinical condition of the eye, the topical anti-inflammatory treatment will be reduced with 1 daily drop per week.
Primary Outcome Measure Information:
Title
Intraocular pressure (IOP)
Description
Postoperative intraocular pressure (IOP) by applanation tonometry
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Best corrected visual acuity
Description
Postoperative best corrected visual acuity in logarithm to the minimal angle of resolution (logMAR)
Time Frame
12 months, 24 months
Title
Visual field
Description
Postoperative changes in visual field by octopus autoperimetry. (MD)
Time Frame
12 months, 24 months
Title
Optical nerve damage
Description
Optical nerve damage, assessed by measuring retinal nerve fiber layer (RNFL) by peripapillary optical coherence tomography (OCT)
Time Frame
12 months, 24 months
Title
Surgical success
Description
The definition of surgical success criteria is dependent on the the severity of visual field defect (MD, mean deviation of visual sensitivity compared to those expected from the age-matched normative database) glaucoma diagnosis and achievement of target pressure without the use of medication (complete success) or with the use of glaucoma medication (qualified success) Ocular hypertension, target <25 mmHg MD < 6 dB, target < 21 mmHg MD 6 dB - 12 dB, target <18 mmHg MD > 12 dB, target < 15 mmHg
Time Frame
12 months, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with primary open-angle glaucoma (POAG), pseudoexfoliation syndrome (PEX), pigment dispersion syndrome (PDS) or ocular hypertension >50 years Women must be postmenopausal. Women are asked if they have menstruated within the preceding 12 months Scheduled to undergo trabeculectomy surgery at the Department of Ophthalmology at Rigshospitalet-Glostrup, Denmark Informed consent to participation and ability to comply with study procedures Exclusion Criteria: Known allergy to any of the contents of the pharmaceuticals (active and in-active ingredients) used in the study Prior intraocular surgery, except from cataract surgery. If cataract surgery has been performed, it should at least be 6 months prior to surgery Medical history of anterior segment dysgenesis, inflammatory/uveitic glaucoma, angle closure glaucoma, neovascular glaucoma and traumatic glaucoma Steroid responders Pregnancy Fertile women, i.e. women who are not menopausal and women who breastfeed Patients in systemic treatment with steroid or NSAID
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniella Bach-Holm, MD, Ph.D.
Organizational Affiliation
Dpt. of Ophthalmology, Rigshospitalet-Glostrup
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Ophthalmology
City
Glostrup
State/Province
Capital Region,
ZIP/Postal Code
2600
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Steroids and/ or Non-steroidal Anti-inflammatory Drugs in the Postoperative Regime After Trabeculectomy.

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