The Effect of Perineural Dextrose Injection in Patients With Ulnar Neuropathy at the Elbow

Ulnar Neuropathies Clinical Trial

Official title:

To Evaluate the Effect of Perineural Dextrose Injection in Patients With Ulnar Neuropathy at the Elbow and to Compare the Control Group

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03737916
• Other study ID #: E171616
• Status: Completed
• Phase: N/A
• Start date: November 18, 2018
• Est. completion date: November 18, 2020

Study information

• Verified date: August 2022
• Source: Ankara Education and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ulnar neuropathy at the elbow (UNE) is the second most common neuropathy and occurs after recurrent or elongated elbow flexion. Diagnosis of UNE depends on clinical symptoms, physical examination, and electrophysiological findings. Imaging methods such as ultrasonography (USG) and magnetic resonance imaging show cross-sectional area and echogenicity of ulnar nerve and give information about to surrounding structures around the ulnar nerve. In mild and moderate cases, conservative treatments are administered up to 6 months, who do not benefit from conservative treatment are referred to surgery. There are not many options for conservative treatment. Activity modification, nerve gliding exercises and night splints are conservative treatment methods. Steroid injection is no longer recommended. Perineural dextrose injection is applied in tendinopathies and entrapment neuropathies (especially carpal tunnel syndrome). In the literature, there is no study showing effect of perineural dextrose injection in patients with UNE. The investigators design a randomized, double-blind, controlled trail to evaluate the effect after ultrasound-guided perineural injection with 5% dextrose in patients with UNE.

Description:

After obtaining written informed consent, patients of clinically diagnosed with UNE 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 normal saline. No additional treatment after injection through the study period. The primary outcome is visual analog scale (VAS) and secondary outcomes include Quick-DASH (Disabilities of Arm, Shoulder and Hand), cross-sectional area (CSA) of the ulnar nerve, motor nerve conduction velocity and distal latency of the ulnar nerve. The evaluation was performed pretreatment as well as on the 2nd week, 1st and 3rd month after the treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: November 18, 2020
• Est. primary completion date: June 18, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Age between 18-65 year-old.
• Neuropathic pain on the ulnar nerve distribution area for at least 1 months
• Diagnosis was confirmed using an electrophysiological studies and ultrasonography

Exclusion Criteria:

• History of trauma to the upper extremity
• Central or peripheral neurologic disease
• Electromyography (EMG)-proven carpal tunnel syndrome, radiculopathy or any other neuropathy
• Pregnancy or any systemic disease that might cause swelling on nerves (e.g., diabetes -mellitus, renal failure, and thyroid disease)
• USG-detected bifid or trifid median nerve, persistent median artery, or space-occupying lesions

Related Conditions & MeSH terms

• Ulnar Neuropathies

Intervention

Other:
• 5 cc 5% Dextrose solution
Ultrasound-guided perineural injection with 5% Dextrose (1cc) to ulnar nerve into the elbow, 2 and 4 cm before and after the elbow (total 5 cc).
• 5 cc salin
Ultrasound-guided perineural injection with salin (1cc) to ulnar nerve into the elbow, 2 and 4 cm before and after the elbow (total 5 cc).

Locations

Country	Name	City	State
Turkey	Basak Mansiz-Kaplan	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Ankara Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline of pain on 2nd week, 1st and 3rd months after treatment: VAS	Using the Visual analog scale (VAS) to measure the pain scale before treatment and multiple time frame after treatment. Recorded on a visual analogue scale (VAS), scores range from 0 to 100 mm, with higher scores indicating worse pain.	Time Frame: Pre-treatment, 2nd week, 1st and 3rd months after treatment
Secondary	Change from baseline in activity and functional status on 2nd week, 1st and 3rd months after treatment.	Using the Quick-DASH to measure the activity and functional status before treatment and multiple time frame after treatment. The Quick-DASH is a shortened version of the DASH Outcome Measure. Instead of 30 items, the QuickDASH uses 11 items to measure physical function and symptoms in people with any or multiple musculoskeletal disorders of the upper limb. The higher scores indicate worse functional status.	Pre-treatment, 2nd week, 1st and 3rd months after treatment
Secondary	Change from baseline in cross-sectional area of the ulnar nerve on 1st and 3th months after treatment.	Using the musculoskeletal ultrasonography to measure the cross-sectional area of the ulnar nerve.	Pre-treatment, 2nd week, 1st and 3rd months after treatment treatment
Secondary	Change from baseline in motor nerve conduction velocity of the ulnar nerve	Using Electromyography to measure the motor nerve conduction velocity (m/sn) of the ulnar nerve	Pre-treatment, 1st and 3rd months after treatment treatment