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Treatment of Calcific Tendinitis by Ultrasound-guided Needle Lavage

M

Martina Hansen's Hospital

Status

Completed

Conditions

Calcific Tendinitis

Treatments

Procedure: Ultrasound guided needle lavage

Study type

Interventional

Funder types

Other

Identifiers

NCT01832376
2012/773

Details and patient eligibility

About

Study population: Subjects with long standing symptoms from calcific tendonitis, non-responsive to other forms of conservative treatment

Study method: A cohort of 50 patients with symptomatic calcific tendonitis will be treated by ultrasound-guided needle lavage. At baseline all study subjects will be assessed by clinical examination, imaging of the shoulder by x-ray and sonography and by the self-report section of the American Shoulder and Elbow Surgeons score (ASES). Follow-up will be performed after 1 and 4 weeks (score only), 3 (clinical, score, ultrasound, x-ray), 6 and 12 months (score only), and after 24 months (clinical, score, ultrasound, x-ray). Patients with insufficient treatment effect will be offered physiotherapy, re-lavage or surgical treatment by acromioplasty.

Purpose of the study: The investigators want to find out

  • if shoulder function, measured by a shoulder score, will increase during follow-up
  • how much of the calcific material can be aspirated (in ml)
  • to which extend the calcific deposit disappears on x-rays and sonographic images
  • how many patients will need surgical treatment

Enrollment

52 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Shoulder pain for at least 6 months, localised laterally on the upper humerus
  • Painful arc
  • Positive Hawkins test and/or Neers tegn for impingement
  • Calcific deposit of >= 5 mm on shoulder x-ray, verified on sonography with a localisation in the supraspinatus or infraspinatus tendon

Exclusion criteria

  • The presence of other local or systemic diseases affecting shoulder function like arthritis, inflammatory arthropathy or instability
  • Symptoms from a cervical root syndrome
  • Sonographic or MRI findings for a rotator cuff tear
  • Earlier surgery in the study shoulder

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

52 participants in 1 patient group

Ultrasound guided needle lavage
Experimental group
Description:
Ultrasound guided needle lavage
Treatment:
Procedure: Ultrasound guided needle lavage

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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