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Comparative effectiveness of ultra-sound guided injections of corticosteroid and perineural dextrose 5% in patients with cubital tunnel syndrome

Comparative effectiveness of ultra-sound guided injections of corticosteroid and perineural dextrose 5% on clinical appearance, function, sonographic and electrodiagnostic findings in patients with cubital tunnel syndrome, a clinical trial study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220929056056N1
Enrollment
22
Registered
2022-12-26
Start date
2023-01-20
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Cubital tunnel syndrome. Lesion of ulnar nerve, unspecified upper limb

Interventions

Intervention 1: First Intervention group: The patients will be placed in a supine position with the shoulder abducted and the elbow flexed at 90°.The ulnar nerve within the cubital tunnel will be iden

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Mild to moderate ulnar nerve entrapment Age of 20-65 years At least 1 month persistence of symptoms and signs

Exclusion criteria

Exclusion criteria: Severe condition Brachial plexus neuropathy History of elbow trauma or operation Rheumatologic disorder Peripheral neuropathy Previous perineural injection Malignancy Coagulopathy Pregnancy Active infection or infection of injection site

Design outcomes

Primary

MeasureTime frame
Upper limb pain. Timepoint: Before intervention, three weeks and twelve weeks later. Method of measurement: Visual Analogue Scale, PRUNE questionnaire.;Sensory and Motor symptoms. Timepoint: Before intervention, three weeks and twelve weeks later. Method of measurement: PRUNE questionnaire.

Secondary

MeasureTime frame
Function of patient. Timepoint: Before intervention, three weeks and twelve weeks later. Method of measurement: PRUNE questionnaire.;Cross-sectional area of ulnar nerve. Timepoint: Before intervention and twelve weeks later. Method of measurement: Ultrasonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Mirhadi

Shiraz University of Medical Sciences

maryam.mirhadii@gmail.com+98 71 3845 4837

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026