Recruiting PHASE1, PHASE2 Glaucoma Following Surgery

New treatment option for Glaucoma Following Surgery

Official title Topical Infliximab in Eyes With Penetrating Keratoplasty

ClinicalTrials.gov ID: NCT05180994

What this study is testing

What is Topical infliximab?

Topical infliximab is an investigational medicine, given as a treatment applied to the skin, being studied as a potential treatment for glaucoma following surgery.

Also referred to as Remicade.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
Penetrating keratoplasty is a cornea surgery involving several inflammatory complications, of which the most important is glaucoma. Researchers wish to determine whether it is safe to administer infliximab (an anti-inflammatory drug) eye drops after surgery, and whether this eye drop could prevent the occurrence of glaucoma.
  • Phase 2: a mid-size study of how well it works

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 80

You may be able to join if

  • Age between 18 and 80 years;
  • First corneal transplant surgery;
  • Capable of providing informed consent;
  • Capable of administering eye medication or access to a caregiver able and willing to administer the eye medication for the patient.

You likely can't join if

  • Active ocular infection;
  • Past corneal transplant (any technique);
  • Advanced glaucoma or macular disease;
  • Active or latent systemic infection (tuberculosis, histoplasmosis, coccidioidomycosis, cytomegalovirus, pneumocystis, aspergillosis or hepatitis B);
  • Malignancy diagnosed in the past 5 years (any kind);
  • Demyelinating disease;
See the full eligibility criteria
Who can join
  • Age between 18 and 80 years;
  • First corneal transplant surgery;
  • Capable of providing informed consent;
  • Capable of administering eye medication or access to a caregiver able and willing to administer the eye medication for the patient.
What rules you out
  • Active ocular infection;
  • Past corneal transplant (any technique);
  • Advanced glaucoma or macular disease;
  • Active or latent systemic infection (tuberculosis, histoplasmosis, coccidioidomycosis, cytomegalovirus, pneumocystis, aspergillosis or hepatitis B);
  • Malignancy diagnosed in the past 5 years (any kind);
  • Demyelinating disease;
  • History or current diabetes mellitus (controlled or uncontrolled) or heart failure (New York Heart Association class III or IV);
  • Pregnancy or breastfeeding;
  • Allergy to infliximab or to a compound of its topical formulation;
  • Significant anomaly of complete blood count or hepatic enzymes;
  • Current or anterior use of anti-TNF-α medication or other anti-inflammatory biologics.

The study team makes the final eligibility decision.

Where it's taking place

  • Montreal, Quebec, Canada

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years to 80 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Montreal, Quebec, Canada. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.