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The Effect Evaluation of Laser Acupuncture in Obesity

The Effect Evaluation of Laser Acupuncture in Obesity

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01975168
Enrollment
200
Registered
2013-11-04
Start date
2013-09-30
Completion date
2015-07-31
Last updated
2013-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

laser acupuncture, obesity

Brief summary

A randomized double-blind placebo-controlled crossover trial is conducted. 200 subjects aged above 20 years with body mass index (BMI) more than 25 kg/m2 are randomly divided into 2 groups (Group 1 and Group 2). Group 1 receives laser acupuncture therapy first while Group 2 receives sham laser acupuncture therapy first. After 12 weeks of treatment and 14 days of washout, Group 1 switch to sham laser acupuncture therapy while Group 2 switch to laser acupuncture for 12 weeks. The subjects are treated with a gallium aluminum arsenide Handylaser Trion, which is used to apply at each of the acupuncture points for 10 seconds every time, 3 times per week. The measurements of outcomes are performed in the beginning, weekly during treatment, and monthly after treatment for 3 months.

Interventions

DEVICEHandylaser Trion laser acupuncture

intervention interval is 3 times per week for 12 weeks

Sponsors

Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Body Mass Index over 25 kg/m2 or Waist girth over 80cm in female, waist girth over 90cm in male

Exclusion criteria

* Pathmakers user * Epilepsy history * Pregnancy * Immuno-inhibiting agents user * Malignancy * Skin contacted disease * Weight controlled agents user during trial period * Eating disorder

Design outcomes

Primary

MeasureTime frameDescription
body composition12 weeksbody weight

Secondary

MeasureTime frame
body mass index12 weeks

Other

MeasureTime frame
body fat12 weeks
waist circumference12 weeks
heart rate12 weeks
blood pressure12 weeks
hip circumference12 weeks

Countries

Taiwan

Contacts

Primary ContactCheng-Che Lin, MD
abcmacoto@gmail.com+8863121101
Backup ContactChen-Cheng Yang, MD
cheng10042001@yahoo.com.tw+886929919132

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026