Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
ID06503302

The Effect of Doppler Ultrasound on Calcified Tendinitis: a Double Blind, Randomized Controlled Trial

Led by Taipei Medical University Shuang Ho Hospital · Updated on 2026-05-01

100

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Calcific tendinitis of the shoulder is a condition where calcium phosphate crystals build up in the rotator cuff tendons, causing pain and reduced shoulder movement that affects quality of life. This research aims to evaluate the usefulness of color Doppler ultrasonography, an imaging technique that shows blood flow and inflammation, in diagnosing and treating calcified tendinitis more effectively. Participants will be randomly assigned to one of two groups: one where doctors use Doppler ultrasound to detect active inflammation in calcifications before an ultrasound-guided injection, and another where Doppler imaging is applied only in non-calcified areas to keep patients unaware of the inflammation status. Both groups receive ultrasound-guided injections as treatment. This is a single-blind, randomized controlled trial led by Taipei Medical University Shuang Ho Hospital with a study period starting in July 2024. During the study, participants will be monitored for the need for a second injection between three days and one week after the first. Researchers will assess pain levels, calcification size, and arm, shoulder, and hand function using questionnaires before treatment, shortly after injection, and within four weeks. These evaluations help determine if using Doppler ultrasound improves treatment outcomes. The study includes adults aged 18 to 80 with chronic shoulder pain and calcifications confirmed by X-ray.

CONDITIONS

Brief Title

The Effect of Doppler Ultrasound on Calcified Tendinitis

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 80 years
  • Chronic shoulder pain lasting more than 1 month
  • Shoulder X-ray showing calcified deposits
Not Eligible

You will not qualify if you...

  • Patient with needle phobia
  • Patient with known allergy to medications like Triamcinolone and Lidocaine

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Between three days to one week

Participants undergo Doppler ultrasound to assess blood flow around calcifications before an ultrasound-guided injection.

1 visit (in-person)

Treatment

Duration - Within the fourth week after the initial ultrasound-guided injection

Participants receive an ultrasound-guided injection based on Doppler ultrasound findings or control procedure without Doppler evaluation.

Up to 2 visits (in-person) including initial injection and possible second injection

Trial Site Locations

Total: 1 location

1

Taipei Medical University-Shuang Ho Hospital, Ministry of Health and Welfare

Taipei, Taiwan, 235

Actively Recruiting

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Research Team

M

Mei Sean Loh

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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Published Research Related To This Trial

Ultrasound Features Associated With Shoulder Complaints: Calcifications Larger Than 6 mm in Young Patients and Positive Doppler Are Associated With Pain.

João Janeiro, Sofia C Barreira, Patrícia Martins...

https://pubmed.ncbi.nlm.nih.gov/34869414

Ultrasound imaging-guided percutaneous treatment of rotator cuff calcific tendinitis: success in short-term outcome.

Alberto Bazzocchi, Patrizia Pelotti, Salvatore Serraino...

https://pubmed.ncbi.nlm.nih.gov/26607641