Ulnar Neuropathy at Elbow
Conditions
Keywords
ulnar neuropathy at elbow, Dextrose, perineural injection
Brief summary
Ulnar neuropathy at elbow (UNE) is the second common peripheral entrapment neuropathy. Although many conservative managements of UNE, the effectiveness of these methods are unsatisfied especial the moderate degree of UNE. Recently, ultrasound-guided perineural injection therapy (PIT) with 5% dextrose is progressively applicated for clinical treatment for entrapment neuropathy. However, current studies have not proved the effects of PIT on peripheral neuropathy because these studies enrolled small number of patients and lacked controlled design. We design a randomized, double-blind, controlled trail to assess the effect after ultrasound-guided PIT with 5% dextrose in patients with mild and moderate UNE.
Detailed description
After obtaining written informed consent, 40 patients, clinically diagnosed with mild or moderate UNE were randomized into intervention or control group. Participants in intervention group received one-session of ultrasound-guided PIT injection with 5cc. 5% dextrose and control group received 2cc 0.9% normal saline+3cc Triamcinolone (30mg) (total 5 cc) ultrasound-guided PIT injection. The primary outcome is Disabilities of the Arm, Shoulder and Hand (DASH) and secondary outcomes include visual analog scale (VAS), cross-sectional area (CSA) of the ulnar nerve, motor nerve conduction velocity of the ulnar nerve, and strength of palmer finger pinch and grasp. The evaluation was performed pretreatment as well as on the 1st, 3rd and 6th month after the treatment.
Interventions
DRUG5% dextrose
Ultrasound-guided 5cc 5% dextrose injection between medial epicondyle and ulnar nerve
DRUG2cc 0.9% normal saline+3cc Triamcinolone (30mg)
Ultrasound-guided 2cc 0.9% normal saline+3cc Triamcinolone (30mg) injection between medial epicondyle and ulnar nerve
DEVICEUltrasound
The ultrasound was used for injection guidance
Sponsors
Tri-Service General Hospital
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
Yes
Inclusion criteria
* Age between 20-80 year-old. * Diagnosis was confirmed using an electrophysiological study
Exclusion criteria
* Cancer * Coagulopathy * Pregnancy * Inflammation status * Cervical radiculopathy * Polyneuropathy, brachial plexopathy * Thoracic outlet syndrome * Previously undergone wrist surgery or steroid injection for ulnar neuropathy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from pain on 1st, 3rd, 6th month after injection | Pre-treatment, 1st, 3rd, 6th month after injection | Digital pain severity or paresthesia/dysthesia was evaluated using visual analog scale (VAS). Pain score scale ranged from 0 to 10, with 10 indicating the most severe pain. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change from severity of symptoms and functional status on 1st, 3rd, 6th month after injection | Pre-treatment, 1st, 3rd, 6th month after injection | Taiwan Disabilities of the Arm, Shoulder and Hand (DASH) contains 11-item disability/symptom scale and each item has five levels of response scoring from 1 to 5. The higher score means more disability or severer symptoms. |
| Change from nerve conduction velocity on 1st, 3rd, 6th month after injection | Pre-treatment, 1st, 3rd, 6th month after injection | Nerve motor conduction velocity of the ulnar nerve before treatment and multiple time frame after treatment. |
| Change from cross-sectional area on 1st, 3rd, 6th month after injection | Pre-treatment, 1st, 3rd, 6th month after injection | Using the musculoskeletal sonogram to measure the cross-sectional area of the ulnar nerve before treatment and multiple time frame after treatment. |
| Change from palmer finger pinch and grasp on 1st, 3rd, 6th month after injection | Pre-treatment, 1st, 3rd, 6th month after injection | The palmer finger pinch and grasp strength was measured using dynamometer (Fabrication Enterprises Inc., USA) before treatment and multiple time frame after treatment. |
Countries
Taiwan
Outcome results
None listed