Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 70Years
All Genders
NCT05474729

Minocycline for Chronic Autoimmune Uveitis

Led by Sun Yat-sen University · Updated on 2023-04-18

10

Participants Needed

1

Research Sites

265 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Autoimmune uveitis is one kind of non-infectious, sight-threatening, relapsing and severe ocular disease. Approximately 20%-25% autoimmune uveitis patients suffer from the dilemma of blindness for the chronic and persistent inflammatory state in the eyes, which results in continuous destroy in the structure of the eyes and gradually leads to irreversible damage on visual function. However, it shows limiting efficacy of current treatment including glucocorticoids, immunosuppressant and biologics for chronic autoimmune uveitis. Minocycline has been regarded to have anti-apoptosis and immunemodulatory function for decades and it has been illustrated to be beneficial in several neuro-degenerative and neuro-inflammatory diseases. This trial aims to investigate the efficacy and safety of minocycline for chronic autoimmune uveitis with retinal degenerative changes.

CONDITIONS

Official Title

Minocycline for Chronic Autoimmune Uveitis

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with autoimmune disease causing vision damage (decreased BCVA or retinal structure loss)
  • Aged 18 to 60 years old
  • Signed informed consent and able to complete all study visits
Not Eligible

You will not qualify if you...

  • Allergy to minocycline or tetracycline antibiotics
  • Abnormal liver, heart, kidney, or thyroid function
  • Currently using glucocorticoids, immunosuppressants, or biologics
  • Pregnant, breastfeeding, or planning pregnancy
  • Using other medications for different diseases

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Zhongshan Ophthalmic Center

Guangzhou, Guangdong, China, 510000

Actively Recruiting

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Research Team

D

Dan Liang

CONTACT

Y

Yuxi Chen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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