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Investigate, Following Cataract Surgery With IOL in Conjunction With Intracanalicular Dexamethasone Insert

W

Wolstan and Goldberg Eye Associates

Status and phase

Completed
Phase 4

Conditions

Glaucoma, Primary Open Angle
Cataract

Treatments

Drug: Intracanalicular Dexamethasone, 0.4 mg insert

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT04465864
DEXTENZA

Details and patient eligibility

About

Randomized, controlled treatment with an intracanalicular dexamethasone (0.4mg) insert following cataract surgery with intraocular lens implant (IOL) combined with minimally invasive glaucoma surgery (MIGS), specifically iStent, iStent inject or KDB in patients with primary open angle glaucoma (POAG) or ocular hypertension (OHTN)

Full description

To determine treatment and patient reported outcomes, following cataract surgery with intraocular lens implant in conjunction with minimally invasive glaucoma surgery (MIGS) more specifically iStent, iStent inject or KDB with an intracanalicular dexamethasone (0.4 mg) insert, inserted four days (+/- 1 day) prior to surgery as compared to insertion on day of surgery. Patients with either primary open angle glaucoma (POAG) or ocular hypertension (OHTN) requiring cataract surgery with IOL implant, will be separated into two groups.

Group 1: intracanalicular dexamethasone (0.4 mg) insertion four days (+/- 1 day) prior to cataract surgery with intraocular lens (IOL) implant and MIGS (iStent, iStent inject or KDB) insertion. (Patient to use antibiotic three days prior to surgery) Group 2: intracanalicular dexamethasone (0.4 mg) insertion on the day of cataract surgery with intraocular lens (IOL) implant and MIGS (iStent, iStent inject or KDB) insertion. (Patient to use antibiotic three days prior to surgery)

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18 years and older
  • Been diagnosed with POAG or OHTN and MIGS (iStent, iStent inject or KDB) has been planned
  • Unilateral or bilateral cataract surgery with IOL has been planned
  • Willing and able to comply with clinic visits and study related procedures
  • Willing and able to sign the informed consent form

Exclusion criteria

  • Patients under the age of 18.

  • Pregnancy (must be ruled out in women of child-bearing age with pregnancy test)

  • Active infectious systemic disease

  • Active infectious ocular or extraocular disease

  • Unobstructed nasolacrimal duct in the study eye(s)

  • Hypersensitivity to dexamethasone

  • Patients being treated with immunomodulating agents in the study eye(s)

  • History of prior ocular surgery, including Lasik or PRK

  • History of ocular inflammation or macular edema

  • Patients being treated with >375mg daily of NSAIDs

    o Patients on doses higher than 375mg of oral NSAIDs will be considered if they discontinue the medication 2 weeks prior to the study start date.

  • Patients taking inconsistent varying doses of an NSAID on a daily basis.

  • Patients being treated with immunosuppressants and/or oral steroids

  • Patients with a corticosteroid implant (i.e. Ozurdex)

  • Patients with severe disease that warrants critical attention, deemed unsafe for the study by the investigator

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Insertion visit 4 days prior
Other group
Description:
Intracanalicular dexamethasone (0.4 mg) insertion four days (+/- 1 day) prior to cataract surgery with intraocular lens (IOL) implant and MIGS (iStent, iStent inject or KDB) insertion. (Patient to use antibiotic three days prior to surgery)
Treatment:
Drug: Intracanalicular Dexamethasone, 0.4 mg insert
Surgical 1 visit day 0
Other group
Description:
Intracanalicular dexamethasone (0.4 mg) insertion on the day of cataract surgery with intraocular lens (IOL) implant and MIGS (iStent, iStent inject or KDB) insertion. (Patient to use antibiotic three days prior to surgery)
Treatment:
Drug: Intracanalicular Dexamethasone, 0.4 mg insert

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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