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Celecoxib for Thyroid Eye Disease

Primary Purpose

Thyroid Eye Disease

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Celecoxib
artificial tears
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Thyroid Eye Disease

Eligibility Criteria

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

Inclusion Criteria:

  • Recent diagnosis of thyroid eye disease (within the past 3 months)
  • Have ocular symptoms or signs of TED with a clinical activity score (CAS) of at least 3

Exclusion Criteria:

  • Pregnancy
  • Previous treatment with corticosteroid for TED for >2wks
  • Previous treatment with orbital radiation for TED
  • Impaired renal function
  • Impaired hepatic function
  • Treatment with antihypertensive medications except beta-blockers
  • History of congestive heart failure, cardiac valvular disease, or coronary artery disease
  • Allergy to NSAID or previous adverse reaction (ie. GI bleeding)
  • Vision loss due to compressive optic neuropathy

Sites / Locations

  • Wilmer Eye Institute, Johns Hopkins University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Celecoxib

Control

Arm Description

Patients who are randomized to treatment with celecoxib 100mg pills by mouth twice a day for 3 months, in addition to standard of care treatment as described under the Control arm

Patients who are randomized to standard treatment (requiring no prescription medication, but standard recommendations such as artificial tears, avoiding cigarette smoke)

Outcomes

Primary Outcome Measures

Thyroid Eye Disease Clinical Activity Score
A clinical score based on examination findings at each clinic visit. Clinical Activity Scores ranged from 0 to 10; 0 = Normal 1-3 = Mild 4-6 = Moderate 7-10 = Severe

Secondary Outcome Measures

Proptosis as Measured in Millimeters With an Exophthalmometer (Right Eye)
A clinical measure of how prominent the eyes are and any change in this measure over the duration of the study, as measured in millimeters with an exophthalmometer.
Proptosis as Measured in Millimeters With an Exophthalmometer (Left Eye)
A clinical measure of how prominent the eyes are and any change in this measure over the duration of the study, as measured in millimeters with an exophthalmometer.
Number of Participants With Ocular Misalignment
Presence or absence of ocular misalignment measured in prism diopters.
Number of Participants With Ocular Misalignment
Presence or absence of ocular misalignment measured in prism diopters.
Number of Participants With Ocular Misalignment
Presence or absence of ocular misalignment measured in prism diopters.
Number of Participants With Ocular Misalignment
Presence or absence of ocular misalignment measured in prism diopters.
Eyelid Retraction as Measured in Millimeters (Right Eye)
A clinical measure of the most common manifestation of thyroid eye disease--change in eyelid retraction as measured in millimeters at each visit over the duration of the study.
Eyelid Retraction as Measured in Millimeters (Left Eye)
A clinical measure of the most common manifestation of thyroid eye disease--change in eyelid retraction as measured in millimeters at each visit over the duration of the study.
Quality of Life as Assessed by a Thyroid Eye Disease Specific Survey of Quality of Life
Thyroid eye disease specific survey of quality of life will be administered, and change in quality of life score over the duration of the study will be measured.

Full Information

First Posted
July 20, 2016
Last Updated
July 15, 2020
Sponsor
Johns Hopkins University
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1. Study Identification

Unique Protocol Identification Number
NCT02845336
Brief Title
Celecoxib for Thyroid Eye Disease
Official Title
An Open Label Trial of Celecoxib in the Treatment of Mild Thyroid Eye Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Terminated
Why Stopped
Poor enrollment
Study Start Date
March 5, 2017 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University

4. Oversight

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

5. Study Description

Brief Summary
Thyroid eye disease (TED) is an autoimmune disorder in which the immune system attacks orbital tissues, resulting in characteristic changes in eyelid position, globe position in the orbit, extraocular muscle balance, and optic nerve function. TED is a potentially blinding disease, and current treatments largely consist of nonspecific reduction of inflammation using corticosteroids or radiation therapy. Regardless of treatment, once TED progresses from its inflammatory phase to a more fibrotic, resolution phase, the orbital changes become fixed and can be modified only by surgery. The investigators propose to treat a cohort of patients with active TED using a selective COX-2 inhibitor, celecoxib, and to compare these patients to an observational control group. The investigators hypothesize that celecoxib will reduce the severity of disease and/or prevent progression to proptosis, diplopia, and corneal exposure or compressive optic neuropathy.
Detailed Description
The investigators intend to use celecoxib, a non-steroidal anti-inflammatory drug approved by the Food and Drug Administration (FDA) for the treatment of pain, osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis, as a treatment for active TED. In vitro data have shown that transformation of orbital fibroblasts into adipocytes is mediated by cyclooxygenase-2 (COX-2), and a case report suggests that COX-2 inhibition can improve TED in the acute phase. Thus, the investigators intend to evaluate the efficacy of COX-2 inhibition in the treatment of active TED and its ability to improve both the acute inflammatory signs and more permanent fibrotic changes of quiescent disease. The investigators will enroll patients with active TED and treat them for 3 months (a characteristic period of disease activity) and compare this to standard treatments for mild active TED (observation, with over the counter interventions such as lubrication with artificial tears) to assess efficacy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thyroid Eye Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Celecoxib
Arm Type
Experimental
Arm Description
Patients who are randomized to treatment with celecoxib 100mg pills by mouth twice a day for 3 months, in addition to standard of care treatment as described under the Control arm
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Patients who are randomized to standard treatment (requiring no prescription medication, but standard recommendations such as artificial tears, avoiding cigarette smoke)
Intervention Type
Drug
Intervention Name(s)
Celecoxib
Other Intervention Name(s)
Celebrex
Intervention Description
celecoxib 100mg PO twice per day for 3 months
Intervention Type
Drug
Intervention Name(s)
artificial tears
Intervention Description
Standard care for mild thyroid eye disease is lubrication with artificial tears (over the counter), avoidance of cigarette smoke.
Primary Outcome Measure Information:
Title
Thyroid Eye Disease Clinical Activity Score
Description
A clinical score based on examination findings at each clinic visit. Clinical Activity Scores ranged from 0 to 10; 0 = Normal 1-3 = Mild 4-6 = Moderate 7-10 = Severe
Time Frame
At baseline, 1, 3 and 6 months
Secondary Outcome Measure Information:
Title
Proptosis as Measured in Millimeters With an Exophthalmometer (Right Eye)
Description
A clinical measure of how prominent the eyes are and any change in this measure over the duration of the study, as measured in millimeters with an exophthalmometer.
Time Frame
At baseline, 1, 3 and 6 months
Title
Proptosis as Measured in Millimeters With an Exophthalmometer (Left Eye)
Description
A clinical measure of how prominent the eyes are and any change in this measure over the duration of the study, as measured in millimeters with an exophthalmometer.
Time Frame
At baseline, 1, 3 and 6 months
Title
Number of Participants With Ocular Misalignment
Description
Presence or absence of ocular misalignment measured in prism diopters.
Time Frame
At baseline
Title
Number of Participants With Ocular Misalignment
Description
Presence or absence of ocular misalignment measured in prism diopters.
Time Frame
At 1 month
Title
Number of Participants With Ocular Misalignment
Description
Presence or absence of ocular misalignment measured in prism diopters.
Time Frame
At 3 months
Title
Number of Participants With Ocular Misalignment
Description
Presence or absence of ocular misalignment measured in prism diopters.
Time Frame
At 6 months
Title
Eyelid Retraction as Measured in Millimeters (Right Eye)
Description
A clinical measure of the most common manifestation of thyroid eye disease--change in eyelid retraction as measured in millimeters at each visit over the duration of the study.
Time Frame
At baseline, 1, 3 and 6 months
Title
Eyelid Retraction as Measured in Millimeters (Left Eye)
Description
A clinical measure of the most common manifestation of thyroid eye disease--change in eyelid retraction as measured in millimeters at each visit over the duration of the study.
Time Frame
At baseline, 1, 3 and 6 months
Title
Quality of Life as Assessed by a Thyroid Eye Disease Specific Survey of Quality of Life
Description
Thyroid eye disease specific survey of quality of life will be administered, and change in quality of life score over the duration of the study will be measured.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Recent diagnosis of thyroid eye disease (within the past 3 months) Have ocular symptoms or signs of TED with a clinical activity score (CAS) of at least 3 Exclusion Criteria: Pregnancy Previous treatment with corticosteroid for TED for >2wks Previous treatment with orbital radiation for TED Impaired renal function Impaired hepatic function Treatment with antihypertensive medications except beta-blockers History of congestive heart failure, cardiac valvular disease, or coronary artery disease Allergy to NSAID or previous adverse reaction (ie. GI bleeding) Vision loss due to compressive optic neuropathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy J McCulley, MD
Organizational Affiliation
Wilmer Eye Institute, Johns Hopkins School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wilmer Eye Institute, Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Celecoxib for Thyroid Eye Disease

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