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Validation of automated sonographic determination of skeletal age in idiopathic adolescent scoliosis using BAUSport™ compared to automated and manual measurement according to Tanner/Whitehouse

Validation of automated sonographic determination of skeletal age in idiopathic adolescent scoliosis using BAUSport™ compared to automated and manual measurement according to Tanner/Whitehouse

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00037118
Enrollment
100
Registered
2025-09-03
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

M41.10

Interventions

Group 1: Children and adolescents with idiopathic scoliosis in whom the determination of skeletal age is indicated undergo both an ultrasonographic and a radiographic examination of the left hand

Sponsors

Asklepios Katharina Schroth Klinik
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: - Participants aged between 10 and 17 years - Idiopathic scoliosis - Medical indication for radiological determination of skeletal age - Patients of Caucasian ethnicity (differences in maturity development between different ethnic groups)

Exclusion criteria

Exclusion criteria: Exclusion criteria: - Patients with malformations of the left hand or who have recently undergone surgery on the left hand - Patients with a bacterial or fungal infection of the left hand - Patients with restricted movement of the left hand - Patients taking medication (high doses of cortisone, high doses of vitamin D, bisphosphonates) that affect bone metabolism or bone mineralisation - Patients who are (possibly) pregnant - Patients who are not fully capable of giving their consent or who lack the capacity to do so, unless this condition is due to their age and the consent of their legal representative or guardian has not been obtained after prior clarification

Design outcomes

Primary

MeasureTime frame
Determination of the validity of automated sonographic measurements in relation to automated radiological and manual measurements according to Tanner/Whitehouse

Secondary

MeasureTime frame
Determination of the reliability of automated sonographic measurement

Countries

Germany

Contacts

Public ContactOmar Zabar

Asklepios Katharina Schroth Klinik

o.zabar@asklepios.com06751874151

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026