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Determination of reference values of Ultrasonographic Tissue Characterization (UTC) measurements in healthy Achilles tendons and evaluation of UTC abnormalities in patients with Achilles tendinopathy

Determination of reference values of Ultrasonographic Tissue Characterization (UTC) measurements in healthy Achilles tendons and evaluation of UTC abnormalities in patients with Achilles tendinopathy - Ultrasonographic Tissue Characterization measurements in Achilles tendons

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32302
Enrollment
140
Registered
2008-05-22
Start date
2009-03-24
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

skeletspierstelsel- en bindweefselaandoeningen. pees-, ligament- en kraakbeenaandoeningen en diagnostiek achillodynia tendon overuse injury

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Asymptomatic Achilles tendons: 1. Age 18-62 year;Symptomatic Achilles tendinopathy: 1. Age 18-62 year 2. Achilles tendon pain for at least 2 months 3. Pain on palpation 2-7 cm proximal to Achilles tendon insertion

Exclusion criteria

Exclusion criteria: asymptomatic Achilles tendons: 1. History of Achilles tendon pain 2. History of tendinopathy at another location 3. Appointment in outpatients clinic because of a problem with the lower extremity 4. Familiair hypercholesterolaemia;symptomatic Achilles tendinopathy: 1. Clinical suspicion of an insertional disorder 2. Clinical suspicion of an Achilles tendon rupture 3. Clinical suspicion of tenosynovitis of the plantar flexors 4. Clinical suspicion sural nerve pathology 5. Clinical suspicion of Peroneal subluxation 6. Clinical suspicion of several internal disorders with an inflammatory origin

Design outcomes

Primary

MeasureTime frame
1.Maximum AP diameter (mm) 2.Distance to the lesion from the tendon insertion (cm) 3.Lesion type (I-IV: Paratenonitis, Tendinosis, Pantendinopathy and Partial rupture) 4.Quantification tendon integrity (Percentage complete tendon fibers, Percentage *waving* fibers, Percentage cellular / fibrillar components, Percentage fluid)

Secondary

MeasureTime frame
In patients with symptomatic Achilles tendinopathy: VISA-A questionnaire (a validated instrument to evaluate the severity of Achilles tendon pain and dysfunction).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)