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April 4, 2026PLoS ONE0 citationsOpen Access

Safety and efficacy of Vectored thermal pulsation, Intense pulsed light, and Eyelid Warm compress therapies (VIEW) for meibomian gland dysfunction: Study design and baseline characteristics of a randomized controlled trial

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ZHZhichao HuHWHanson Yiu Man WongECEmily Hoi Ying Chan

Key Points

  • To evaluate the safety and efficacy of vectored thermal pulsation, intense pulsed light with meibomian gland expression, and eyelid warm compress therapies for managing meibomian gland dysfunction.
  • Conducted a 3-arm, assessor-masked, randomized controlled trial.
  • 360 symptomatic mild to moderate MGD subjects recruited and randomized into three intervention groups.
  • Group-A received one session of vectored thermal pulsation, Group-B four sessions of intense pulsed light plus meibomian gland expression, and Group-C used eyelid warm compress twice daily for 15 months.
  • Topical artificial tears prescribed to all subjects throughout the study.
  • Subjects assessed nine times over a total of 16 months using multiple evaluation methods.
  • 374 subjects enrolled, and 372 subjects aged 54.4 ± 14.7 years were analyzed.
  • Mean tear film break-up time at baseline was 3.1 ± 1.7 seconds.
  • Data indicates variability in therapeutic efficacy across the different treatments.

Abstract

Background Meibomian gland dysfunction (MGD) is one of the most prevalent chronic eye diseases, characterized by meibomian gland obstruction and abnormal meibum secretion both in quantity and quality. Objective To assess the efficacy and safety of vectored thermal pulsation (VTP), intense pulsed light plus meibomian gland expression (IPL + MGX), and eyelid warm compress (EW). Methods This is a 3-arm, assessor-masked, randomized controlled trial. 360 symptomatic mild to moderate MGD subjects would be recruited and randomized into 3 intervention groups. Subjects from Group-A, Group-B, and Group-C would be treated with one-session VTP (at baseline), four-session IPL + MGX (at baseline, month-1, month-2, and month-3 visits), and twice-daily EW for 15 months, respectively. All subjects would be prescribed topical artificial tears (Hypromellose, 0.3% w/v) to be used as frequently as needed from wash-out (1 month before baseline) to endpoint (month-15 visit). Subjects would be assessed 9 times throughout a total of 16-month study period. Five self-administered questionnaires would be collected each time in random order. Masked observers would conduct examinations using slit-lamp biomicroscopy, LipiView® II, and Keratograph 5M machines. The eye with worse MGD would be selected and analyzed as the study eye. Tear film break-up time (TFBUT) at month-6 and month-15 visits are the primary outcomes. Results 374 subjects were enrolled and randomized into three groups, and 372 subjects (aged 54.4 ± 14.7 years) were finally analyzed. The mean of TFBUT time at baseline was 3.1 ± 1.7 seconds. Conclusion This is the first head-to-head comparison of three physical treatments for mild to moderate MGD on their therapeutic efficacy, safety, longevity and compliance in a randomized controlled trial setting.

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Cite This Study

Hu et al. (2026) studied this question.

synapsesocial.com/papers/69d0ae94659487ece0fa4901https://doi.org/10.1371/journal.pone.0342421
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