Carpal Tunnel Syndrome Clinical Trial
— CTSOfficial title:
A Randomised Controlled Double Blind Trial Of Therapeutic Ultrasound in Carpal Tunnel Syndrome (CTS)
Verified date | January 2018 |
Source | East Kent Hospitals University NHS Foundation Trust |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
Status | Completed |
Enrollment | 40 |
Est. completion date | January 3, 2018 |
Est. primary completion date | February 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | East Kent Hospitals University NHS Foundation Trusts | Canterbury | Kent |
Lead Sponsor | Collaborator |
---|---|
East Kent Hospitals University NHS Foundation Trust |
United Kingdom,
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. — View 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. — View Citation
Bland JD. A neurophysiological grading scale for carpal tunnel syndrome. Muscle Nerve. 2000 Aug;23(8):1280-3. — View Citation
Bland JD. Do nerve conduction studies predict the outcome of carpal tunnel decompression? Muscle Nerve. 2001 Jul;24(7):935-40. — View 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. — View Citation
Foley JL, Little JW, Vaezy S. Effects of high-intensity focused ultrasound on nerve conduction. Muscle Nerve. 2008 Feb;37(2):241-50. — View 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;(1):CD003219. Review. — View 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. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | Baseline, 7th week, 6 months and end of 12months | |
Secondary | 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. | 7th week, 6 months and end of 12 months | |
Secondary | Nerve Conduction Studies | Changes in Nerve Conduction Studies grading. | Baseline,7th week, 6 months and end of 12 months | |
Secondary | Ultrasound Imaging of Wrist(s) | Measurements of Cross section Area (CSA)of the median nerve at the wrist(s). | Baseline, 7th week, 6 and 12 months |
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