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Ultrasound Therapy for Carpal Tunnel Syndrome (CTS) (CTS)

Primary Purpose

Carpal Tunnel Syndrome

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
EMS Therasonic 460 Primo Ultrasound therapy
Sponsored by
East Kent Hospitals University NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carpal Tunnel Syndrome focused on measuring Ultrasound therapy, Nerve Conduction studies, Boston and Levine Questionnaire, Neutral Angle Wrist Splint, Canterbury CTS scale

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male and female participants aged between 18 and 90 years with mild carpal tunnel syndrome (Canterbury NCS grades 1-3).
  • No Previous treatment history other than splinting and use of over the counter NSAIDs.

Exclusion Criteria:

  • Subjects diagnosed with peripheral neuropathy, secondary entrapment neuropathies diabetes mellitus, rheumatoid disease, acute trauma.
  • Previous carpal tunnel surgery.
  • Pregnancy or lactating.
  • Patients with known HIV infection.
  • Other serious medical or psychiatric illness currently ongoing, or experienced within the past three months, that in the opinion of the investigator would compromise the study.
  • Patients unable to comply with the protocol requirements, including severe alcohol and drug use.

Sites / Locations

  • East Kent Hospitals University NHS Foundation Trusts

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Sham Ultrasound regimen

Real Ultrasound therapy

Arm Description

A switch in the transducer circuit allows mock ionisation as a result no ultrasound emitted.

Pulsed mode ultrasound therapy

Outcomes

Primary Outcome Measures

Changes in Boston/Levine subjective Symptom score
Improvement in the Boston/Levine subjective Symptom score at completion of Ultrasound treatment(real or sham), a decrease of at least 1.04 points being considered a clinically significant change.

Secondary Outcome Measures

Functional status score
Improvement in functional status score, participants overall opinion of outcome, duration of Ultrasound therapy effect and relapses will be assessed for one year.
Nerve Conduction Studies
Changes in Nerve Conduction Studies grading.
Ultrasound Imaging of Wrist(s)
Measurements of Cross section Area (CSA)of the median nerve at the wrist(s).

Full Information

First Posted
April 26, 2012
Last Updated
January 30, 2018
Sponsor
East Kent Hospitals University NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT01590745
Brief Title
Ultrasound Therapy for Carpal Tunnel Syndrome (CTS)
Acronym
CTS
Official Title
A Randomised Controlled Double Blind Trial Of Therapeutic Ultrasound in Carpal Tunnel Syndrome (CTS)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
June 2012 (Actual)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
January 3, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
East Kent Hospitals University NHS Foundation Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Carpal Tunnel Syndrome (CTS) is a recognisable pattern of symptoms and signs, which are caused by compression of the median (middle) nerve as it passes through the carpal tunnel at the wrist. This condition affects individuals by causing pain, numbness, tingling sensations and sometimes weakness in the fingers and may extend to shoulder and neck areas. The cause for most cases is unknown (idiopathic) though some common conditions are associated with an increased incidence, including obesity, pregnancy, hypothyroidism, arthritis, diabetes, and trauma. Diagnosis is primarily clinical and the condition is easily recognised from the characteristic symptoms in straightforward cases but diagnostic support is provided by investigations such as nerve conduction studies and ultrasound imaging. Treatment may include splinting, local steroid injection at wrist, activity modification,physical or occupational therapy (controversial), medications, and surgery. Treatment with local therapeutic ultrasound has been suggested to be effective but existing trials are inconclusive. Wrist splinting is only partially effective with a success rate of 34%, Steroid injection is followed by frequent relapses and there remains uncertainty about the safety of serial injections. Surgery is effective but has a small but significant incidence of permanent complications. Any demonstrably effective and safe addition to the therapeutic options would be a significant advance in treatment. Therapeutic ultrasound at present appears a promising option, having a very good safety record but so far uncertain evidence of efficacy. In our trial patients, with mild carpal tunnel syndrome, confirmed by nerve conduction studies, will all be given wrist splints so that no patients will be left untreated. They will be randomly allocated to either therapeutic or sham ultrasound therapy (20 sessions over 7 weeks) and followed up for 1year. The patients, operators of the ultrasound equipment and assessors will all be blind to treatment allocation. The effect of treatment on symptoms will be assessed using a validated questionnaire and nerve conduction studies will be repeated at completion of the ultrasound treatment, 6 and 12 months. This study is designed to find out to whether therapeutic ultrasound is an effective treatment for carpal tunnel syndrome (CTS).
Detailed Description
Carpal tunnel syndrome (CTS) is the commonest peripheral nerve disorder in the UK. Average annual incidences (per 100 000) were 139.4 for women and 67.2 for men in East Kent, UK. It has significant economic impact, on average having the largest recuperation period of all injuries / illness that require days away from work. It causes tingling, numbness or pain in the distribution of the median nerve (the thumb, index, and middle fingers, and half the ring finger) that is often worse at night and causes wakening. The pathology of idiopathic CTS is a non-inflammatory fibrosis of the subsynovial connective tissue surrounding the flexor tendons but the causes are not fully understood. Many treatments have been proposed but reviews performed by the Cochrane collaboration have found firm evidence in support of only: Surgical decompression of the carpal tunnel. Steroid therapy (local injection or systemic administration). Neutral angle wrist splinting. None of the available evidence based treatments for CTS are entirely satisfactory. Splinting is only partially effective with a success rate of 34%, Steroid injection is followed by frequent relapses and there remains uncertainty about the safety of serial injections. Surgery results in a small but significant incidence of permanent morbidity from complications. Any demonstrably effective and safe addition to the therapeutic options would be a significant advance. Of the many candidate treatments, therapeutic ultrasound at present appears the most promising and is therefore the subject of this proposal Therapeutic ultrasound has a very good safety record and is essentially non-invasive. In this trial, patients with mild carpal tunnel syndrome, confirmed by nerve conduction studies, will all be given wrist splints. They will be randomly allocated to either real or sham ultrasound therapy (20 sessions over 7 weeks) and followed up for 1 year. The effect of treatment on symptoms will be assessed using a validated questionnaire and nerve conduction studies will be repeated at completion of the ultrasound treatment at 7th week and further after 6 and 12 months time. This will be a randomised, double blind, single-centre, clinical trial conducted by East Kent Hospitals University Foundation Trusts (Kent and Canterbury Hospital), with follow-up for 1 year from completion of treatment. Following randomisation, patients will be required to attend the clinic for 20 sessions over a 7 weeks period (5x weekly for 2 weeks then 2x weekly for 5 weeks).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carpal Tunnel Syndrome
Keywords
Ultrasound therapy, Nerve Conduction studies, Boston and Levine Questionnaire, Neutral Angle Wrist Splint, Canterbury CTS scale

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sham Ultrasound regimen
Arm Type
Placebo Comparator
Arm Description
A switch in the transducer circuit allows mock ionisation as a result no ultrasound emitted.
Arm Title
Real Ultrasound therapy
Arm Type
Active Comparator
Arm Description
Pulsed mode ultrasound therapy
Intervention Type
Device
Intervention Name(s)
EMS Therasonic 460 Primo Ultrasound therapy
Other Intervention Name(s)
Ultrasound treatment
Intervention Description
1MHz / 1.0W/cm square probe for 15 minutes per session for 20 sessions.
Primary Outcome Measure Information:
Title
Changes in Boston/Levine subjective Symptom score
Description
Improvement in the Boston/Levine subjective Symptom score at completion of Ultrasound treatment(real or sham), a decrease of at least 1.04 points being considered a clinically significant change.
Time Frame
Baseline, 7th week, 6 months and end of 12months
Secondary Outcome Measure Information:
Title
Functional status score
Description
Improvement in functional status score, participants overall opinion of outcome, duration of Ultrasound therapy effect and relapses will be assessed for one year.
Time Frame
7th week, 6 months and end of 12 months
Title
Nerve Conduction Studies
Description
Changes in Nerve Conduction Studies grading.
Time Frame
Baseline,7th week, 6 months and end of 12 months
Title
Ultrasound Imaging of Wrist(s)
Description
Measurements of Cross section Area (CSA)of the median nerve at the wrist(s).
Time Frame
Baseline, 7th week, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female participants aged between 18 and 90 years with mild carpal tunnel syndrome (Canterbury NCS grades 1-3). No Previous treatment history other than splinting and use of over the counter NSAIDs. Exclusion Criteria: Subjects diagnosed with peripheral neuropathy, secondary entrapment neuropathies diabetes mellitus, rheumatoid disease, acute trauma. Previous carpal tunnel surgery. Pregnancy or lactating. Patients with known HIV infection. Other serious medical or psychiatric illness currently ongoing, or experienced within the past three months, that in the opinion of the investigator would compromise the study. Patients unable to comply with the protocol requirements, including severe alcohol and drug use.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kamalakannan Jothi
Organizational Affiliation
East Kent Hospitals University NHS Foundation Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jeremy Bland
Organizational Affiliation
East Kent Hospitals University NHS Foundation Trust
Official's Role
Study Chair
Facility Information:
Facility Name
East Kent Hospitals University NHS Foundation Trusts
City
Canterbury
State/Province
Kent
ZIP/Postal Code
CT13NG
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
9862296
Citation
Oztas O, Turan B, Bora I, Karakaya MK. Ultrasound therapy effect in carpal tunnel syndrome. Arch Phys Med Rehabil. 1998 Dec;79(12):1540-4. doi: 10.1016/s0003-9993(98)90416-6.
Results Reference
background
PubMed Identifier
9529407
Citation
Ebenbichler GR, Resch KL, Nicolakis P, Wiesinger GF, Uhl F, Ghanem AH, Fialka V. Ultrasound treatment for treating the carpal tunnel syndrome: randomised "sham" controlled trial. BMJ. 1998 Mar 7;316(7133):731-5. doi: 10.1136/bmj.316.7133.731.
Results Reference
background
PubMed Identifier
12535461
Citation
O'Connor D, Marshall S, Massy-Westropp N. Non-surgical treatment (other than steroid injection) for carpal tunnel syndrome. Cochrane Database Syst Rev. 2003;2003(1):CD003219. doi: 10.1002/14651858.CD003219.
Results Reference
background
PubMed Identifier
10918269
Citation
Bland JD. A neurophysiological grading scale for carpal tunnel syndrome. Muscle Nerve. 2000 Aug;23(8):1280-3. doi: 10.1002/1097-4598(200008)23:83.0.co;2-y.
Results Reference
background
PubMed Identifier
14638888
Citation
Bland JD, Rudolfer SM. Clinical surveillance of carpal tunnel syndrome in two areas of the United Kingdom, 1991-2001. J Neurol Neurosurg Psychiatry. 2003 Dec;74(12):1674-9. doi: 10.1136/jnnp.74.12.1674.
Results Reference
background
PubMed Identifier
11410921
Citation
Bland JD. Do nerve conduction studies predict the outcome of carpal tunnel decompression? Muscle Nerve. 2001 Jul;24(7):935-40. doi: 10.1002/mus.1091.
Results Reference
background
PubMed Identifier
8176515
Citation
Banta CA. A prospective, nonrandomized study of iontophoresis, wrist splinting, and antiinflammatory medication in the treatment of early-mild carpal tunnel syndrome. J Occup Med. 1994 Feb;36(2):166-8. doi: 10.1097/00043764-199402000-00012.
Results Reference
background
PubMed Identifier
18041054
Citation
Foley JL, Little JW, Vaezy S. Effects of high-intensity focused ultrasound on nerve conduction. Muscle Nerve. 2008 Feb;37(2):241-50. doi: 10.1002/mus.20932.
Results Reference
background
Links:
URL
http://www.carpal-tunnel.net/
Description
Click here for more information about carpal tunnel syndrome and canterbury patients can keep in touch with specialist through this web page.

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Ultrasound Therapy for Carpal Tunnel Syndrome (CTS)

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