Radiculopathy Clinical Trial
Official title:
Efficacy of Ultrasound Versus Short Wave Diathermy in the Treatment of Lumbar Disc Herniation: a Randomised Control Study
Verified date | November 2023 |
Source | Baskent University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Chronic low back pain is a common problem which results in reduced functionality, quality of life and general well being. Conservative treatment includes patient education, exercise, maintaining a healthy body mass index and appropriate modifications to activities of daily living. Physical modalities are used to support the mainstay of treatment and include superficial heat, transcutaneous electrical nerve stimulation (TENS), ultrasound, short wave diathermy , traction, and complimentary therapies. In the clinical practice of the investigators, diathermy, in the form of ultrasound and short wave, is used to heat deeper tissues, increase tissue elasticity and metabolic rate and reduce pain and muscle spasm. The medical literature to date states that further studies are required to compare the efficacy of different diathermy modalities in the treatment of lower back pain. The aim of this study was to compare the efficacy of ultrasound to that of short wave diathermy and a treatment program which does not include diathermy in the treatment of a slipped disc.
Status | Completed |
Enrollment | 82 |
Est. completion date | December 31, 2021 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility | Inclusion Criteria: - 1)Age 20-60 - 2)Presenting to the Baskent University Faculty of Medicine Physical Medicine and Rehabilitation Department outpatient clinic - 3) history of low back pain for greater than three months - 4) Aetiology of back pain lumbar disc herniation based on history, examination and computed tomography/ magnetic resonance imaging (protruded, extruded disc) Exclusion Criteria: - 1)lower extremity neurological deficit, 2) infectious, inflammatory, metabolic, neoplastic, abdominal, pelvic aetiology of back pain. 3) a history of vertebral fracture, spinal surgery, spondylolisthesis 4) heat intolerance/medical contraindication to thermal treatment 5) presence of metal prosthesis |
Country | Name | City | State |
---|---|---|---|
Turkey | Baskent University Faculty of Medicine, Ankara Hospital | Ankara |
Lead Sponsor | Collaborator |
---|---|
Baskent University |
Turkey,
Ahmed MS, Shakoor MA, Khan AA. Evaluation of the effects of shortwave diathermy in patients with chronic low back pain. Bangladesh Med Res Counc Bull. 2009 Apr;35(1):18-20. doi: 10.3329/bmrcb.v35i1.2320. — View Citation
Chou R, Huffman LH; American Pain Society; American College of Physicians. Nonpharmacologic therapies for acute and chronic low back pain: a review of the evidence for an American Pain Society/American College of Physicians clinical practice guideline. Ann Intern Med. 2007 Oct 2;147(7):492-504. doi: 10.7326/0003-4819-147-7-200710020-00007. Erratum In: Ann Intern Med. 2008 Feb 5;148(3):247-8. — View Citation
Chou R, Qaseem A, Snow V, Casey D, Cross JT Jr, Shekelle P, Owens DK; Clinical Efficacy Assessment Subcommittee of the American College of Physicians; American College of Physicians; American Pain Society Low Back Pain Guidelines Panel. Diagnosis and treatment of low back pain: a joint clinical practice guideline from the American College of Physicians and the American Pain Society. Ann Intern Med. 2007 Oct 2;147(7):478-91. doi: 10.7326/0003-4819-147-7-200710020-00006. Erratum In: Ann Intern Med. 2008 Feb 5;148(3):247-8. — View Citation
Fiore P, Panza F, Cassatella G, Russo A, Frisardi V, Solfrizzi V, Ranieri M, Di Teo L, Santamato A. Short-term effects of high-intensity laser therapy versus ultrasound therapy in the treatment of low back pain: a randomized controlled trial. Eur J Phys Rehabil Med. 2011 Sep;47(3):367-73. Epub 2011 Jun 8. — View Citation
Jegede KA, Ndu A, Grauer JN. Contemporary management of symptomatic lumbar disc herniations. Orthop Clin North Am. 2010 Apr;41(2):217-24. doi: 10.1016/j.ocl.2010.01.003. — View Citation
Kamper SJ, Apeldoorn AT, Chiarotto A, Smeets RJ, Ostelo RW, Guzman J, van Tulder MW. Multidisciplinary biopsychosocial rehabilitation for chronic low back pain: Cochrane systematic review and meta-analysis. BMJ. 2015 Feb 18;350:h444. doi: 10.1136/bmj.h444. — View Citation
Oral A, Ketenci A. Physical Medicine and Rehabilitation Approaches in the Management of Radicular Low Back Pain. A review of the Evidence and Current Recommendations. Turkish Journal of Physlcai and Rehabilitation Medicine 59:57-68, 2013
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in level of pain | visual analogue scale (VAS) score from 0 to 10cm for current pain. 0= no pain 10= the worst pain imaginable | Before treatment, 2 weeks after the commencement of treatment, 6 weeks after the commencement of treatment, 14 weeks after the commencement of treatment | |
Secondary | Change in level of Disability | Modified Oswestry Low Back Pain Disability Questionnaire. The Revised Oswestry Disability Index is a condition specific outcome measure for low back pain. The index consists of ten questions with six possible responses regarding the patient's back pain, (scored from 0-5), including the severity of pain and impact on activities of daily living. The minimum obtainable score is 0, the maximum obtainable score is 50. This score is then used to calculate the index percentage using the formula: [total score/(no. of questions answered x 5)]100. The higher the percentage, the greater the level of disability due to low back pain. The minimal detectable change (90% confidence interval)is 10%, change of less than 10% maybe attributed to measurement error. | Before treatment, 2 weeks after the commencement of treatment, 6 weeks after the commencement of treatment, 14 weeks after the commencement of treatment | |
Secondary | Change in health related quality of life | Short Form 36 (SF-36).The SF 36 is a generic health survey which assesses health concepts that are pertinent to functional status and well-being such as physical function, bodily pain, role limitations due to emotional and physical problems. The sub scale values are reported: physical functioning, bodily pain, vitality, general health, social functioning, emotional role, physical role, mental health. The lowest and highest possible raw score for the subscales are as follows: physical functioning 10-30, physical role 4- 8, bodily pain 2-12, general health 5-25, vitality 4-24, social functioning 2-10, emotional role 3-6, mental health 5-30. Higher values signify better well being in all subgroups. The raw score is then used to calculate the 'transformed scale: Transformed scale= [(actual raw score- lowest possible raw score)/possible raw score range]100 | Before treatment, 6 weeks after the commencement of treatment, 14 weeks after the commencement of treatment |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03733886 -
Burst Spinal Cord Stimulation for Neuropathic Pain.
|
N/A | |
Completed |
NCT04169477 -
Comparison of Two Modes of Transcutaneous Electrical Nerve Stimulation (TENS) in Chronic Neuropathic Radiculalgia
|
N/A | |
Completed |
NCT02265848 -
High Frequency Stimulation Trials in Patients With Precision Spinal Cord Stimulator System
|
Phase 4 | |
Not yet recruiting |
NCT05487690 -
Application of 3D Printing Guide Plate in Spinal Minimally Invasive and Interventional Surgeries
|
N/A | |
Recruiting |
NCT04909138 -
Intermittent Dosing of Dorsal Root Ganglion Stimulation as an Alternate Paradigm to Continuous Low-Frequency Therapy
|
N/A | |
Completed |
NCT05533723 -
Comparison Between Endoscopic Epidural Neuroplasty and Percutaneous Epidural Neuroplasty in Low Back and Radicular Pain
|
||
Not yet recruiting |
NCT06041347 -
Learning Curve for the Visualization of Sacral Plexus on TVS
|
||
Completed |
NCT02939482 -
A Study Comparison of Clinical Outcome After Different Rate of Infusion in Caudal Epidural Steroid Injection
|
N/A | |
Recruiting |
NCT05732818 -
Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nuclectomy 3
|
N/A | |
Active, not recruiting |
NCT04559295 -
Bone Marrow Concentrate (BMC) Injection in Intervertebral Discs
|
Phase 2/Phase 3 | |
Completed |
NCT02644421 -
Clinical Trial to Evaluate the Safety and Analgesic Efficacy of VVZ-149 in Lumbar Radiculopathy (Sciatica)
|
Phase 1 | |
Recruiting |
NCT06193265 -
Management of Lumbar Discectomy by Endoscopy and Conventional Microscopic Discectomy
|
||
Recruiting |
NCT05145842 -
The Effect of Combination of Ultrasound and Flouroscopy Guidance in Caudal Epidural Injections
|
N/A | |
Withdrawn |
NCT03327272 -
Impact of Local Steroid Application in Extreme Lateral Lumbar Interbody Fusion
|
Phase 3 | |
Withdrawn |
NCT02196883 -
Steroid Injections Given at the "Level of MRI Pathology" Versus at the "Level of Clinical Symptoms" to See if One is More Effective Than the Other.
|
N/A | |
Terminated |
NCT01850771 -
Regenexx™ PL-Disc Versus Steroid Epidurals for Lumbar Radiculopathy
|
N/A | |
Completed |
NCT02130258 -
Somatosensory Profiling in Radicular Pain Patients And it's Correlation With Treatment Outcome
|
N/A | |
Withdrawn |
NCT05347108 -
Real-Time Accurate Pathology Inspection and Decompression Study
|
||
Active, not recruiting |
NCT05696470 -
Fusion Rates of 3D Printed Porous Titanium Cages in Three and Four Level ACDFs
|
||
Recruiting |
NCT05952167 -
Evaluation of the Impact of Tractions vs. Placebo Tractions in Patients With Cervical Radiculopathy
|
N/A |