Laser Acupuncture on Dry Eye and Sjögren's Syndrome-related Dry Eye Symptoms (LADESJS)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age20-75
SponsorTaipei Veterans General Hospital, Taiwan

About this trial

This randomized, double-blind, placebo-controlled clinical trial aims to evaluate the efficacy of adding laser acupuncture at Fengchi (GB20), Zanzhu (BL2), Hegu (LI4), and Quchi (LI11) acupoints to standard care for the treatment of dry eye symptoms in both Sjögren's Syndrome-related dry eye (SJS-DES) and non-Sjögren's Syndrome-related dry eye (Non-SJS-DES) populations. A total of 140 dry eye patients will be recruited and divided into two groups: 70 participants with SJS-DES and 70 with Non-SJS-DES. Participants will be randomly assigned into three groups: Sham+LA group (60 participants receiving 4 weeks of placebo laser acupuncture followed by 4 weeks of active laser acupuncture), LA+LA group (60 participants receiving 4 weeks of active laser acupuncture followed by another 4 weeks of active laser acupuncture), and a Waiting List group (20 participants receiving no laser acupuncture treatment). Each session will target the Fengchi (GB20), Zanzhu (BL2), Hegu (LI4), and Quchi (LI11) acupoints bilaterally, performed twice a week. The total study period is 8 weeks, and the treatment efficacy will be assessed at the end of the 8-week treatment. The Waiting List group (20 participants) will not receive any laser acupuncture treatment during this period. Efficacy will be evaluated using the Numerical Rating Scale (NRS), Schirmer's test, Ocular Surface Disease Index (OSDI), EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI), Traditional Chinese Medicine (TCM) tongue diagnosis, TCM pulse diagnosis, TCM constitution questionnaire, TCM heart rate variability analysis, nailfold microcirculation assessment, and iris examination. This study aims to investigate the impact of laser acupuncture on dry eye symptom improvement and the potential markers that differentiate between SJS-DES and Non-SJS-DES patients. The goal is to develop a comprehensive integrated care model for early screening, diagnosis, and personalized treatment plans for Dry Eye Syndrome and Sjögren's Syndrome, achieving the ultimate objective of "Holistic Health Care."

Eligibility criteria

Qualifiers

aged between 20 and 75 years

Schirmer's test less than 10 mm/5 min

Disqualifiers

Pregnancy

With eye inflammation or infectious eye disease

Accepted operation of eye

Sjögren's syndrome

Trial design

Treatments tested in this trial

  • Laser acupuncture (LA)
  • Numerical Rating Scale (NRS)
  • Schirmer's test
  • Ocular Surface Disease Index (OSDI)
  • EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI)
  • Traditional Chinese Medicine (TCM) tongue diagnosis
  • Traditional Chinese Medicine (TCM) pulse diagnosis
  • Traditional Chinese Medicine (TCM) constitution questionnaire
  • Traditional Chinese Medicine (TCM) heart rate variability analysis
  • nailfold microcirculation assessment
  • iris examination
  • Sham Laser Acupuncture

Treatment groups

140 Participants
are divided into 5 treatment groups