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OpenTrials
Completed

NCT Number: NCT04115800

Liposomal Sirolimus in Dry Eye Disease

Dry eye disease is a very frequent pathology that importantly affects the quality of life of patients; in spite of the common use of eye lubricants to ameliorate symptoms, there is still a large number of patients who do not present improvement of the disease or they worsen. Although its etiology is varied, the imbalance of the immune system plays a substantial role in the development of dry eye disease. Rapamycin or sirolimus is an anti-inflammatory and immunomodulatory drug that has an enormous potential in ocular surface pathologies such as dry eye disease. The aim of the present study is to determine the effectiveness and security of subconjunctival application of a new formulated drug of liposomal sirolimus in patients with moderate and severe dry eye disease. This is a randomized placebo-controlled double blind clinical trial. Patients presenting data of moderate or severe dry eye disease will be randomized into two groups. One group will receive additional to the conventional treatment, subconjunctival injections of liposomal sirolimus; meanwhile the other group will receive subconjunctival placebo injections. After intervention the effectiveness and the security of the liposomal sirolimus will be evaluated.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Instituto de Oftalmología

Mexico City, 06800, Mexico

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects with moderate or severe Dry Eye
  • Subjects with OSDI score > 22
  • Subjects with Van Bijsterveld staining score >4
  • Subjects that accept to participate in the study

Exclusion criteria

  • Subjects with refraction surgery antecedents
  • Subjects with ophthalmic surgery six months previous to the study
  • Subjects with Lagophthalmos
  • Subjects with facial paralysis antecedents
  • Subjects with herpetic keratitis
  • Subjects using isotretinoin
  • Pregnant subjects
  • Subjects in lactating period
  • Subjects with allergy or intolerant to the drug
  • Subjects with hepatic disorders
  • Subjects with abnormal thoracic X rays

Treatment and study plan

Liposomal Sirolimus

Drug

Subconjunctival injections of liposomal sirolimus in patients with conventional treatment with moderate and severe dry deye disease

Primary outcomes

  1. Ocular Surface Disease Index (OSDI)

    Time frame: Six weeks after intervention

    The OSDI is assessed on a scale of 0 to 100, with higher scores representing greater disability. The index demonstrates sensitivity and specificity in distinguishing between normal patients and patients with dry eye disease. The OSDI is a valid and reliable instrument for measuring dry eye disease severity (normal, mild to moderate, and sever) and effect on vision -related function.

Sponsors and collaborators

Lead sponsor

Instituto de Oftalmología Fundación Conde de Valenciana

Other

Registry information

Official study title

Subconjunctival Treatment of Liposomal Sirolimus as a Treatment for Dry Eye Disease

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Oct 4, 2019
Registry last updated
Feb 10, 2021

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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