Recruiting PHASE3 Nasolacrimal Duct Obstruction

New treatment option for Nasolacrimal Duct Obstruction

Official title Artificial Tears to Prevent Nasolacrimal Duct Obstruction in Patients Treated With Radioactive Iodine for Thyroid Cancer

ClinicalTrials.gov ID: NCT05999630

What this study is testing

What is Artificial Tears Methylcellulose?

Artificial Tears Methylcellulose is an investigational medicine, being studied as a potential treatment for nasolacrimal duct obstruction.

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
The association of radioiodine therapy for the treatment of thyroid cancer with nasolacrimal duct obstruction has been well documented in the medical literature. Prior case reports have documented radioactive iodine detection in the tears of patients following radioiodine therapy.
  • Phase 3: a large, late-stage study

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

Who can take part

Ages 18 and older. Healthy volunteers may be eligible.

You may be able to join if

  • Radio-iodine therapy for thyroid cancer
  • Radioiodine therapy ≥150 mCi
  • Age 18 or older

You likely can't join if

  • Use of eye drops, other than artificial tears
  • History of periocular trauma with tear duct involvement/lacrimal gland trauma
  • History of lacrimal drainage disease: canaliculitis, dacryocystitis
  • Prior radiotherapy
  • Current or prior use of chemotherapy drugs (i.e. 5-fluorouracil, docetaxel)
  • Medical conditions that predispose to NLD stenosis (i.e. sarcoidosis, granulomatosis with polyangiitis, chronic lymphocytic leukemia)
See the full eligibility criteria
Who can join
  • Radio-iodine therapy for thyroid cancer
  • Radioiodine therapy ≥150 mCi
  • Age 18 or older
What rules you out
  • Use of eye drops, other than artificial tears
  • History of periocular trauma with tear duct involvement/lacrimal gland trauma
  • History of lacrimal drainage disease: canaliculitis, dacryocystitis
  • Prior radiotherapy
  • Current or prior use of chemotherapy drugs (i.e. 5-fluorouracil, docetaxel)
  • Medical conditions that predispose to NLD stenosis (i.e. sarcoidosis, granulomatosis with polyangiitis, chronic lymphocytic leukemia)
  • Nasolacrimal duct obstruction at baseline

The study team makes the final eligibility decision.

Where it's taking place

  • Nashville, Tennessee, United States

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 and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Nashville, Tennessee, United States. 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.