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Completed

NCT Number: NCT00755183

Safety and Efficacy Study of a Testosterone Eye Drop for the Treatment of Meibomian Gland Dysfunction

The objective of this study is to assess the safety and efficacy of testosterone 0.03% ophthalmic solution compared to vehicle for the treatment of meibomian gland dysfunction.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Ophthalmic Research Associates

Andover, Massachusetts, 01810, United States

About this study

Meibomian gland secretion plays a crucial role in the health of the ocular surface and function of the tear film. The lipid secreted by the meibomian glands has many crucial roles: 1) to retard evaporation from the preocular surface; 2) lower the surface tension of tears; 3) prevent spill-over of tears from the lid margin; 4) prevent the contamination of the tear film by sebaceous lipids; 5) prevent damage to the skin of the lid margin. In dry eye syndrome, blepharitis, meibomian gland dysfunction, and meibomitis the glands are the central pathophysiology of disease and thus a potential target for therapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(subjects must):

  • Be ≥ 60 years of age
  • Have a corrected visual acuity of LogMAR +0.5 (ETDRS)
  • Have a documented history of Meibomian Gland Dysfunction
  • Have a TFBUT ≤ 5 seconds
  • Have an ocular discomfort score ≥ 1
  • Have an IOP ≤ 25 mmHg at Visit 1 in both eyes
  • Report use of and/or desire to use an artificial tears

Exclusion criteria

(subjects may not):

  • Have contraindications to the use of the study medications
  • Have a known allergy or sensitivity to the study medications
  • Have any ocular infections, or active ocular inflammation
  • Have used ocular medications within 24 hours prior to Visit 1
  • Be a current contact lens wearer
  • Require the use of any other ophthalmic medication, other than tear substitutes and study medication provided, for the duration of the trial
  • Have used systemic or topical antihistamines or steroids 48 hours prior to Visit 1 or require the use of systemic or topical antihistamines or steroids during the course of the study
  • Have a history of prostate cancer

Treatment and study plan

testosterone ophthalmic solution

Drug

testosterone ophthalmic solution for 128 days

vehicle of testosterone ophthalmic solution

Drug

vehicle of testosterone ophthalmic solution for 128 days

Primary outcomes

  1. Meibomian Gland Secretion Appearance at Visit 4 (Day 168)

    Time frame: 168 days

    The average of the secretion color, quality, and viscosity of the worst gland in the worst eye. All scales were numerical analog, 0-3, where 0=normal and 3=worst.

  2. Ocular Discomfort Score at Visit 4

    Time frame: 168 days

    Ocular Discomfort Score on a 0-4 scale where 0=none and 4=constant discomfort at Visit 4 (Day 168)

Sponsors and collaborators

Lead sponsor

ORA, Inc.

Industry

Registry information

Official study title

A Single-Center, Double-Masked, Randomized, Vehicle Controlled Study to Evaluate the Safety and Efficacy of Testosterone 0.03% Ophthalmic Solution Compared to Vehicle for the Treatment of Meibomian Gland Dysfunction

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Sep 18, 2008
Registry last updated
Oct 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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