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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02990962
Other study ID # PIT for CTS
Secondary ID
Status Completed
Phase N/A
First received December 9, 2016
Last updated April 23, 2018
Start date December 2016
Est. completion date April 1, 2018

Study information

Verified date April 2018
Source Tri-Service General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Carpal tunnel syndrome (CTS) is the most common peripheral entrapment neuropathy with involving compression of the median nerve in the carpal tunnel. Rather than other progressive disease, CTS is characterized by remission and recurrence. Although many conservative managements of CTS, the effectiveness of these methods is insignificant or only persist for a short duration including steroid injection. Recently, the ultrasound-guided perineural injection with 5% dextrose was widely used for entrapment neuropathy with positive benefit. The investigators design a randomized, double-blind, controlled trail to assess the effect of ultrasound-guided perineural injection with 5% dextrose in patients with CTS and compared with steroid injection.


Description:

After obtaining written informed consent, patients of clinically diagnosed with CTS were randomized into intervention and control group. Participants in intervention group received one-session ultrasound-guided perineural injection with 5% dextrose and control group received one-session ultrasound-guided perineural injection with steroid. No additional treatment after injection through the study period. The primary outcome is visual analog scale (VAS) and secondary outcomes include Boston Carpal Tunnel Syndrome Questionnaire (BCTQ), cross-sectional area (CSA) of the median nerve, sensory nerve conduction velocity of the median nerve, and finger pinch strength. The evaluation was performed pretreatment as well as on the 2nd week, 1st, 2nd, 3rd and 6 month after the treatment.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date April 1, 2018
Est. primary completion date April 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Age between 20-85 year-old.

- Diagnosis was confirmed using an electrophysiological study and ultrasonography

Exclusion Criteria:

Cancer

- Coagulopathy

- Pregnancy

- Inflammation status

- Cervical radiculopathy

- Polyneuropathy, brachial plexopathy

- Thoracic outlet syndrome

- Previously undergone wrist surgery or steroid injection for CTS

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
5% dextrose
Ultrasound-guided perineural injection with 5% dextrose (5cc) between carpal tunnel and surrounding median nerve with hydrodissection.
1cc 2% Xylocaine+4cc Triamcinolone (40mg)
Ultrasound-guided perineural injection with1cc 2% Xylocaine+4cc Triamcinolone (40mg) between carpal tunnel and surrounding median nerve with hydrodissection.

Locations

Country Name City State
Taiwan Department of Physical Medicine and Rehabilitation, Tri-Service General Hospital Taipei Neihu District

Sponsors (1)

Lead Sponsor Collaborator
Tri-Service General Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (5)

Armstrong T, Devor W, Borschel L, Contreras R. Intracarpal steroid injection is safe and effective for short-term management of carpal tunnel syndrome. Muscle Nerve. 2004 Jan;29(1):82-8. — View Citation

Girlanda P, Dattola R, Venuto C, Mangiapane R, Nicolosi C, Messina C. Local steroid treatment in idiopathic carpal tunnel syndrome: short- and long-term efficacy. J Neurol. 1993;240(3):187-90. — View Citation

Mulvaney SW. Ultrasound-guided percutaneous neuroplasty of the lateral femoral cutaneous nerve for the treatment of meralgia paresthetica: a case report and description of a new ultrasound-guided technique. Curr Sports Med Rep. 2011 Mar-Apr;10(2):99-104. — View Citation

Tsui BC, Kropelin B. The electrophysiological effect of dextrose 5% in water on single-shot peripheral nerve stimulation. Anesth Analg. 2005 Jun;100(6):1837-9. — View Citation

Tsui BC, Wagner A, Finucane B. Electrophysiologic effect of injectates on peripheral nerve stimulation. Reg Anesth Pain Med. 2004 May-Jun;29(3):189-93. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline of pain on 2nd week, 1st, 2nd, 3rd and 6 month after the treatment. Using the Visual analog scale (VAS) to measure the pain scale before treatment and multiple time frame after treatment. Pre-treatment, 2nd week, 1st, 2nd, 3rd and 6th month after injection
Secondary Change from baseline of severity of symptoms and functional status on 2nd week, 1st, 2nd, 3rd and 6 month after the treatment. Using the Boston Carpal Tunnel Syndrome Questionnaire to measure the symptoms and functional status before treatment and multiple time frame after treatment Pre-treatment, 2nd week, 1st, 2nd, 3rd and 6th month after injection
Secondary Change from baseline of cross-sectional area of the median nerve on 2nd week, 1st, 2nd, 3rd and 6 month after the treatment. Using the musculoskeletal sonogram to measure the cross-sectional area of the median nerve. Pre-treatment, 2nd week, 1st, 2nd, 3rd and 6th month after injection
Secondary Change from baseline of nerve conduction velicity on 2nd week, 1st, 2nd, 3rd and 6 month after the treatment. Nerve motor conduction velocity of the ulnar nerve before treatment and multiple time frame after treatment. Pre-treatment, 2nd week, 1st, 2nd, 3rd and 6th month after injection
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