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Vitamin B12 and Dextrose for Median Nerve Hydrodissection

The Effects of Vitamin B12 and Dextrose on the Ultrasound-guided Median Nerve Hydrodissection

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05423028
Enrollment
120
Registered
2022-06-21
Start date
2021-12-07
Completion date
2024-12-31
Last updated
2024-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome

Brief summary

Carpal tunnel syndrome is the most common peripheral entrapment neuropathy of the upper limb. Previous experiments found that ultrasound-guided median nerve hydrodissection with 5% dextrose water could ameliorate the condition of carpal tunnel syndrome. Oral administration of vitamin B 12 had been reported to reduce the discomfort from peripheral neuropathy although the level of evidence is not strong. This prospective, double-blind randomized control trial aims to compare the effects of different kinds of the injection agents on carpal tunnel syndrome.

Interventions

Peri- median nerve injection for hydrorelease and decompression

Sponsors

National Cheng-Kung University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age between 20-80 year-old. * Diagnosis (carpal tunnel syndrome) was confirmed using an electrophysiological study.

Exclusion criteria

* Previously undergone wrist surgery or steroid injection for CTS * Thrombocytopenia * Coagulopathy * Inflammation status * Polyneuropathy * Brachial plexopathy * Cervical radiculopathy * Autoimmune disease * Malignancy * Pregnancy Thoracic outlet syndrome

Design outcomes

Primary

MeasureTime frameDescription
Change of Boston Carpal Tunnel Syndrome QuestionnairePre-treatment, 1st, 3rd, 6th month after injectionMeasure the severity of symptoms and functional status before and after treatment

Secondary

MeasureTime frameDescription
Visual analog scale of pain and tinglingPre-treatment, 1st, 3rd, 6th month after injectionMeasure the pain and tingling scale before treatment and after treatment. (0 is for not at all pain/tingling, and 100 is for extremely pain/tingling.)
Cross-sectional area of the median nervePre-treatment, 1st, 3rd, 6th month after injectionUsing the ultrasound to measure the cross-sectional area of the median nerve before and after treatment
Median nerve elastographyPre-treatment, 1st, 3rd, 6th month after injectionUsing the ultrasound to measure the elastography of the median nerve before and after treatment
Median nerve conduction velocity and amplitudePre-treatment, 1st, 6th month after injectionAntidromic sensory nerve conduction velocity and amplitude of the median nerve before and after treatment

Countries

Taiwan

Contacts

Primary ContactYao-Hong Guo, MD, MSc
drprps@gmail.com886-6-2353535

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026