Abstract: Introduction: Knee osteoarthritis (KOA) is one of the most common causes of chronic pain and disability. In addition, many studies have shown that laser acupuncture (LA) has a great analgesic effect and minimal side effects. This study aims to evaluate the efficacy and safety of LA combined with knee exercises (KE) in patients with KOA.

Methods: A pilot randomized controlled trial was conducted on 60 patients with KOA at Le Van Thinh Hospital in Ho Chi Minh City from May 2021 to September 2022. Patients were randomly allocated to LA group (n = 30) with KE combined LA or the therapeutic ultrasound (TU) group (n = 30) with KE combined with TU in 4 weeks. The outcome measurements were visual analog scale (VAS) scores and knee range of motion (ROM). The data were collected at 5 time points: T0 (baseline) and after every week of treatment.

Results: After a 4-week treatment, the VAS score of patients in LA groups decreased from 6(5-6) to 3 cm (2-4) (p < 0.01) but was not significantly different when compared to patients in TU groups. In contrast, there is an improvement in the ROM score of patients, from 132.5 (130 – 140) to 140 (140 – 140) with the KOA, and has significantly different when compared to patients in TU groups (p < 0.05).

Conclusion: LA combined with KE exhibited equivalent analgesic effects and increased knee ROM in patients KOA after 2, 3, and 4-week treatment.

Background and Aim: Carpal Tunnel Syndrome (CTS) is a common pathology that affects the quality of human life. It is essential to promote clinical intervention studies. Our initial step in this study focused on the cure for CTS and the safety of Laser Acupuncture (LA), which is a type of acupuncture uses low-level laser instead of metal acupuncture needles.

Method: This is a before-after interventional study based on a group of 38 CTS patients, ranging from mild to moderate. Intervention using LA 5 times per week for 4 weeks, using low-level laser with a continuous wavelength of 655 nm, wattage of 5 mW/point, dose of 6 J/point, and direction perpendicular to the skin surface, in 10 pressure points on the affected hand, including PC4, PC6, PC7, PC8, LI4, LI10, LI1, HT3, HT7, LU10. The change in the Symptom Severity Scale (SSS), Functional Status Scale (FSS) through the Boston Carpal Tunnel Syndrome Questionnaire (BCTQ) and adverse events were monitored to assess the effectiveness and safety of LA.

Results: At the second and fourth weeks, respectively, the SSS score decreased from 28 (27-33) to 14 (14-21) and 12 (11-13); this difference was statistically significant (p<0001). Similarly, the FSS score decreased from 13 (13-15) to 8 (8-10), 8 (8-8), and the difference was statistically significant (p<0001). Following the intervention, 37% (CI 95%, 23-53%) of patients experienced complete symptom recovery and 100% experienced complete functional recovery. No side effects were noted during the treatment.

Conclusion: LA was initially shown to be safe and effective in the treatment of CTS by improving symptoms and rehabilitation.