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High and Low Dose High-intensity Laser Therapy Lateral Epicondylitis

Comparison of the Effects of High and Low Dose High-intensity Laser Therapy in Patients With Lateral Epicondylitis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07342426
Enrollment
45
Registered
2026-01-15
Start date
2026-01-12
Completion date
2026-12-06
Last updated
2026-01-21

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

Conditions

High Intensity Laser, High Intensity Laser Therapy, Lateral Epicondylitis, Tennis Elbow

Keywords

treatment

Brief summary

High-intensity laser therapy has gained increasing attention in recent years as a therapeutic modality. It is a non-invasive treatment that can reduce pain, increase local blood circulation, and promote tissue repair. The higher energy output of high-intensity laser therapy also have deeper tissue penetration. Several studies have investigated the effects of high-intensity laser therapy on lateral epicondylitis, and the existing literature indicates that, compared with other treatment modalities, high-intensity laser therapy is more effective in improving pain and quality of life in patients with lateral epicondylitis. However, the dosage, duration, and treatment frequency applied in previous studies vary considerably. The therapeutic effects of high-intensity laser therapy may therefore be influenced by treatment dosage. Consequently, the purpose of this study is to compare the effects of two different dosages of high-intensity laser therapy on patients with lateral epicondylitis.

Interventions

DEVICEHigh intensity laser therapy

Using high-intensity laser therapy applying on the affected area.

DEVICEInfarred ray therapy system

Using infarred ray therapy applying on affected area for 15 minutes.

Using transcutaneous electrical nerve stimulator on the affected area fior 15 minutes.

Sponsors

Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients diagnosed with lateral epicondylitis by physician 2. Disease duration of less than three months 3. Adults aged above 18 years with full decision-making capacity

Exclusion criteria

1. Patients who have received treatments other than standard treatment to the affected area within past three months 2. Patients with contraindication for rehabilitation therapy 1. Photosensitivity 2. Sensory impairment 3. Implanted cardiac pacemaker 4. Pregnancy 5. Malignancy 3. Patients with a history of surgery on the affected elbow 4. Patients with cervical radiculopathy

Design outcomes

Primary

MeasureTime frameDescription
Pain intensityFrom enrollment to the end of treatment at 4 weeksUsing visual analog scale to measure pain intensity. Score from 0 to 10. Score 0 means no pain and score 10 indicates highest pain.

Secondary

MeasureTime frameDescription
Grip strengthFrom enrollment to the end of treatment at 4 weeksUsing dynanometer to measure grip strength
Quality of lifeFrom enrollment to the end of treatment at 4 weeksUsing Quick disabilities of the Arm, Shoulder, and hand scale (also known as Quick DASH) to measure quality of life of participants. Scale contains 11 questions. Each question scored from 1 to 5, higher score indicates higher degree of disability.

Countries

Taiwan

Contacts

CONTACTCHENG-CHANG LU
cclu0880330@gmail.com+886 975357331
CONTACTMIN-HAO TSAI
petertsai0702@gmail.com+886 908011166

Outcome results

None listed

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