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Comparison of Triamcinolone Injection and TENS for Long Head of the Biceps Tendinopathy

Comparison of Ultrasound-Guided Triamcinolone Injection and Transcutaneous Electrical Nerve Stimulation for the Treatment of Long Head of the Biceps Brachii Tendinopathy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07817433
Enrollment
42
Registered
2026-09-14
Start date
2025-01-06
Completion date
2026-02-11
Last updated
2026-09-14

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

Conditions

Long Head of Biceps Brachii Tendinopathy

Brief summary

This randomized clinical trial compared ultrasound-guided triamcinolone injection and transcutaneous electrical nerve stimulation (TENS) in patients with long head of the biceps brachii tendinopathy. Participants in both groups also received a supervised physiotherapy exercise program. Pain, shoulder-related pain and disability, ultrasonographic findings, and clinical test results were assessed at baseline and at 1 and 3 months after treatment.

Interventions

DEVICETranscutaneous Electrical Nerve Stimulation (TENS)

Conventional transcutaneous electrical nerve stimulation (TENS) was applied at a frequency of 200 Hz and a pulse duration of 200 μs for 15 minutes per session, for a total of 15 sessions.

DRUGTriamcinolone Acetonide and Lidocaine Hydrochloride

A single ultrasound-guided peritendinous injection of 1 mL triamcinolone acetonide (40 mg/mL) mixed with 1 mL lidocaine hydrochloride (20 mg/mL) was administered around the long head of the biceps tendon.

Sponsors

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to 74 Years
Healthy volunteers
No

Inclusion criteria

* Age \>18 years and \<75 years. * Provision of written informed consent. * Long head of the biceps brachii tendinopathy confirmed by ultrasonography (USG) or magnetic resonance imaging (MRI). * Shoulder pain lasting longer than 1 month. * Failure of previous medical treatment.

Exclusion criteria

* Long head of the biceps brachii tendon rupture confirmed by ultrasonography (USG) or magnetic resonance imaging (MRI). * Wound and/or infection at the intervention site. * Steroid injection for the same diagnosis within the previous 3 months. * Known allergy to triamcinolone and/or lidocaine. * Sensory impairment in the shoulder or upper extremity. * Uncontrolled diabetes mellitus. * Diagnosis of epilepsy. * Full-thickness rotator cuff tear confirmed by ultrasonography (USG) or magnetic resonance imaging (MRI).

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale (VAS) for PainBaseline, 1 month, and 3 monthsPain intensity was assessed using a 10-cm Visual Analog Scale (VAS). Pain was evaluated both at rest and during movement. Scores range from 0 (no pain) to 10 (worst imaginable pain), with higher scores indicating greater pain intensity.

Secondary

MeasureTime frameDescription
Shoulder Pain and Disability Index (SPADI)Baseline, 1 month, and 3 monthsShoulder pain and disability were assessed using the Shoulder Pain and Disability Index (SPADI), which includes pain and disability subscales. The total score ranges from 0 to 100, with higher scores indicating greater shoulder pain and disability.
Maximum diameter of the long head of the biceps tendonBaseline, 1 month, and 3 monthsThe maximum diameter of the long head of the biceps brachii tendon was measured by musculoskeletal ultrasonography at the site of greatest tendon thickness and recorded in millimeters (mm).
Peritendinous fluid around the long head of the biceps tendonBaseline, 1 month, and 3 monthsPeritendinous fluid was measured by ultrasonography at the site of greatest effusion between the tendon and tendon sheath and recorded in millimeters (mm). Minimal probe compression was applied during measurement.
Increased vascular signal in the long head of the biceps tendonBaseline, 1 month, and 3 monthsVascular signal in the long head of the biceps tendon region was assessed using Doppler ultrasonography. Any increase in vascular signal detected along the bicipital groove was considered positive. The result was recorded as positive or negative.
Speed TestBaseline, 1 month, and 3 monthsThe Speed test was used to evaluate pathology of the long head of the biceps tendon. Test results were recorded as positive or negative.
Yergason TestBaseline, 1 month, and 3 monthsThe Yergason test was used to evaluate pathology of the long head of the biceps tendon. Test results were recorded as positive or negative.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORYasin Demir, MD

University of Health Sciences Türkiye, Gülhane Faculty of Medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 15, 2026