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
Topical antibiotics (standard therapy) group
Overall
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
Topical antibiotic
|
Outcomes |
Primary outcome:
Secondary outcomes:
|
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 |