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A Randomized, Double-Blind, Placebo-Device Controlled, and Parallel Designed Study to Assess the Efficacy of Laser Acupuncture on Low Back Pain

A Randomized, Double-Blind, Placebo-Device Controlled, and Parallel Designed Study to Assess the Efficacy of Laser Acupuncture on Low Back Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0001314
Enrollment
56
Registered
2014-12-16
Start date
2013-11-04
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Medical Device : Laser acupuncture treatment group: The laser acupuncture consists of laser irradiation device and 4-channel probes with cupping (Solco-LF100, Solco Biomedical Co. Ltd., Pyeongtaek Kor

Sponsors

Korea Institute of Oriental Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Minimum pain intensity on the visual analogous scale for pain (VAS, 0-100mm) 30mm. 2. Diagnosis of low back pain 3. Voluntary participation who clearly understood purpose and characteristics of the clinical trials signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Voluntary participations who were using devices which can be susceptible by electromagnetic field such as pace makers, hearing aid. 2. Volunteers who have severe pain are impossible to participate in clinical trials. 3. Volunteers who was diagnosed fractures, severe disc herniation, spinal tumors that is required immediate treatment and inspection. 4. Volunteers who are taking medication that may affect the clinical trials, such as corticosteroids, anticonvulsants, anti-inflammatory drugs. 5. Pregnant volunteers. 6. Volunteers who have ever been experienced side effects, due to using physical stimulation therapy. 7. Patients who have significant physical and mental deficiencies are impossible to clearly understand the clinical trials procedure. 8. Recently in a month, patients who have participated the clinical trials of another intervention.

Design outcomes

Secondary

MeasureTime frame
Change of pressure pain threshold (PPT) ;Change of EuroQol (EQ-5D) ;Change of patient's global impression of change (PGIC) ;All-cause adverse events after laser acupuncture treatments

Primary

MeasureTime frame
Change of VAS

Countries

Korea, Republic of

Contacts

Public ContactBoncho Ku

Korea Institute of Oriental Medicine

secondmoon@kiom.re.kr+82-42-868-9589

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026