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Outcome of conservatively treated supraspinatus tendon ruptures in consideration of muscular atrophy rated with contrast-enhanced ultrasound

Outcome of conservatively treated supraspinatus tendon ruptures in consideration of muscular atrophy rated with contrast-enhanced ultrasound - CEUS Suspraspinatus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00016533
Enrollment
50
Registered
2019-01-18
Start date
2019-05-02
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

M75.1

Interventions

Group 1: Patients with MRI-assisted diagnosis of supraspinatus tendon rupture and indication for conservative treatment are examined with contrast enhanced ultrasound of the shoulder before and after

Sponsors

Universitätsmedizin Rostock
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with MRI-assisted diagnosis of supraspinatus tendon rupture and indication for conservative treatment

Exclusion criteria

Exclusion criteria: •Inability, to understand the essence of this study •Other rotator cuff defects •Operations or strong impairment of the contralateral shoulder •Earlier operations at the effected shoulder •Tumor •Infection •Known intolerance to SonoVue® •Severe heart failure (NYHA III and IV), Right-Left shunt, uncontrollable hypertension •Severe lung diseases, ARDS and severe pulmonary arterial hypertension •Myocardial infarction in the past 14 days •Age: under 18 years •Pregnancy or breast-feeding period

Design outcomes

Primary

MeasureTime frame
Perfusion of the M. supraspinatus before and after 6 weeks of physiotherapy; measured with CEUS (contrast enhanced ultrasound)

Secondary

MeasureTime frame
Clinical examination including different scores regarding shoulder function (i.a. ASES, SST, Constant score), Assessment of pain with VAS, power measurement (Isobex); further parameters collected during ultrasound examination. All parameters are collected at inclusion and after 6 weeks of standardized treatment with physiotherapy.

Countries

Germany

Contacts

Public ContactMalte Jäschke

Universitätsmedizin Rostock; Institut für Diagnostische und Interventionelle Radiologie, Kinder- und Neuroradiologie

malte.jaeschke@med.uni-rostock.de+49 (0)381 494-9201

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026