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Efficacy of High-intensity Laser Therapy (HILT) in the Patients With Cervical Disc Herniation

B

Baskent University Ankara Hospital

Status

Completed

Conditions

Cervical Disc Herniation

Treatments

Other: Exercise
Device: High Intensity Laser Therapy
Device: Ultrasound
Device: Transcutaneous nerve stimulation (TENS)

Study type

Interventional

Funder types

Other

Identifiers

NCT05474625
E-946003339-604.01.02-38865

Details and patient eligibility

About

The worldwide prevalence of neck pain is between 16.7-75.1%, it has been seen at an increasing rate in recent years due to sedentary living conditions.

Pharmacological treatment, neck collar, traction, manual therapy, interventional injection techniques, surgical treatment and conventional physical therapy methods such as hotpack, ultrasound, TENS (Transcutaneous electrical nerve stimulation), vacuum interference, exercise are applied in the treatment of neck pain.

In recent years, High Intensity Laser Therapy (HILT) has been used as a painless and non-invasive physical therapy agent. It received FDA approval in 2002 for HILT in the treatment of variety of musculoskeletal disorders.

There are a few studies in the literature investigating the efficacy of HILT in chronic neck pain. There is only one study investigating the efficacy of HILT in cervical disc herniation. In this study, the efficacy of HILT and ultrasound-TENS in the treatment of neck pain caused by cervical disc herniation has been compared, but the results of the exercise control group and long-term follow-up were not available.

The aim of this randomized controlled trial is to evaluate the short and long-term efficacy of HILT treatment using improvement in the pain, range of motion, activities of daily living and functionality of the cervical spine in patients with cervical disc herniation. In group 1, only exercises will be applied; in the group 2, HILT will be applied in addition to exercise; in the group 3, hotpack, TENS, ultrasound will be applied in addition to exercises.

Enrollment

150 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with cervical disc herniation diagnosed by MRI whose symptoms started for at least 3 months ago
  • Not receiving physical therapy and rehabilitation in the last 3 months
  • Not taking any medications such as analgesics, anti-inflammatoires or muscle relaxants for the treatment of symptoms.

Exclusion criteria

  • patients with major psychiatric disease, cervical spine surgery and rheumatological disease; pacemaker users; those who were injected with local corticosteroids; pregnant women; cancer patients

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

150 participants in 3 patient groups

Exercise Group
Active Comparator group
Description:
Only exercises
Treatment:
Other: Exercise
High Intensity Laser Therapy(HILT) Group
Active Comparator group
Description:
Exercises+HILT
Treatment:
Other: Exercise
Device: High Intensity Laser Therapy
Conventional Physiotherapy Group
Active Comparator group
Description:
Exercise+Hotpack+Transcutaneous nerve stimulation (TENS)+Ultrasound
Treatment:
Other: Exercise
Device: Ultrasound
Device: Transcutaneous nerve stimulation (TENS)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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