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Minocycline Treatment for Cystoid Macular Edema (MINOCME)

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Sun Yat-sen University

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Minocycline
Cystoid Macular Edema

Treatments

Drug: minocycline

Study type

Interventional

Funder types

Other

Identifiers

NCT05474950
MINOCME

Details and patient eligibility

About

Cystoid macular edema (CME) is one of sight-threatening, immune-related ocular diseases. The efficacy of current treatments for CME (anti-VEGF, glucocorticoids and other agents) are limiting. Minocycline, acting as a broad-spectrum antibiotic, is among tetracycline family and recently, its immunomodulatory and anti-apoptosis function has been replied to several immune diseases and degenerative diseases. This study aims to explore the efficacy and safety of minocycline for CME.

Enrollment

5 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participant diagnosed with CME.
  • Participant aged from 18-60 years old.
  • Participant that signed the informed consent document and is able to complete the following visits.

Exclusion criteria

  • Participant is allergy to minocycline or tetracyclines.
  • Participant has no contraindications of minocycline or tetracyclines.
  • Participant has an abnormal function of liver, heart, kidney and thyroid.
  • Female that is pregnant, breast-feeding or planning to become pregnant.
  • Participant that is currently using other medications.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

minocycline
Experimental group
Treatment:
Drug: minocycline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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