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. 2020 Mar 18;2020(3):CD013559. doi: 10.1002/14651858.CD013559

NCT02958514.

Trial name or title Effectiveness: comparison of two kinds of treatment in treating dry eye caused by meibomian gland dysfunction
Methods Study design: randomised controlled trial
Study grouping: parallel group
Exclusions after randomisation? Not applicable
Percentage of participant follow‐up: not applicable
Study duration (of intervention): 12 weeks with 3 cycles of IPL of 4 weeks' interval and artificial tears 4 times daily
Was a sample size calculation reported: no
Participants Baseline characteristics
IPL group
  • Number of participants (number of eyes): not reported

  • Sex: not reported

  • Age: not reported


Topical antibiotics (standard therapy) group
  • Number of participants (number of eyes): not reported

  • Sex: not reported

  • Age: not reported


Overall
  • Number of participants (number of eyes): 20 (not reported)

  • Sex: not reported

  • Age: not reported


Inclusion criteria: people with dry eye syndrome and diagnosed as MGD
Exclusion criteria: infection or inflammatory disease; ocular surgical history within last 3 months; Sjogren's syndrome
Significant pretreatment baseline differences? Not applicable
Severity of dry eye: not reported
Interventions IPL
  • Description: IPL (Diamond Q4 by DermaMed Solutions) with Xenon flash lamp to emit wavelengths of light 400–1200 nm.

  • Duration: 12 weeks (3 cycles of 4 weeks)

  • Co‐interventions: artificial tears 4 times daily


Topical antibiotic
  • Description: tobramycin and dexamethasone ophthalmic ointment at night

  • Duration: 12 weeks

  • Co‐interventions: artificial tears 4 times daily

Outcomes Primary outcome:
  • OSDI score at study completion (mean 6 months).


Secondary outcomes:
  • concentrations of inflammatory cytokines such as IL‐1, IL‐6 and IL‐8 at study completion;

  • tear BUT at study completion;

  • corneal fluorescein stain at study completion;

  • eyelid ester discharge ability score at study completion;

  • ester trait ratings at study completion.

Starting date First posted: 8 November 2016; no further updates.
Contact information Responsible party: Hong Qi
Peking University Third Hospital, 49 Huayuan N Road, Haidian District, Beijing, China
Notes Open‐label trial