Early mobilization after hip reconstructive surgery in children - A prospective randomized clinical trial

Not Applicable

Recruiting

• Conditions: Q65.0; Q65.9; Congenital dislocation of hip, unilateral; Congenital deformity of hip, unspecified

• Registration Number: DRKS00016861
• Lead Sponsor: Kepler Universitätsklinikum Linz

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-03-04
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

children and adolescents Age 4-14 years
diagnosis: dysplasia of the hip with indication für hip reconstructive surgery; surgical methods are Pemberton/Dega osteotomy, Salter osteotomy, derogation-varisation osteotomy; Indications for surgery are: Reimers migration index 40% or higher or 25-40% with progression, Tönnis classification II or higher or AC-Index above the Tönnis-standard.
informed consent of Patient and parent
standardized questionnaire before surgery, after 6 and 12 weeks, radiological assessment 6 and 12 weeks after surgery

Exclusion Criteria

no informed consent
denial of usage of obtained data
withdrawal of informed consent
non-compliance

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
standardised questionnaire (SF-36, EQ-5D, CPCHILD) on termination of immobilization 6 weeks postoperatively

Secondary Outcome Measures

Name	Time	Method
unplanned premature termination of immobilization due to adverse event (skin problems, neurological deficits, infection, compliance problems, material failure); Counting and documentation of adverse events