Health Condition 1: C00-D49- Neoplasms
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Tata Memorial Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1. Rotationplasty patients with at least 1 year of follow up. 2. Patients of any age and any sex shall be recruited for functional outcome and gait analyses. 3. Patients who have reached skeletal maturity (physeal fusion seen on plain X-Ray) for primary outcome measure of knee length discrepancy.
Exclusion criteria
Exclusion criteria: 1. Rotationplasty patients with less than 1 year follow up. 2. Those who present with local and/or systemic relapse.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Limb length discrepancy as measured by a difference in knee heights on standard of care X- ray (radiographs). Knee height will be measured from ASIS (anterior superior iliac spine) to the center of the talus on a scannogram taken in an upright weight bearing stance with the prosthesis in use and pelvis squared. The normal limb knee length shall be measured from ASIS to the center of the knee joint.Timepoint: Single point assessment after enrollment. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Patient or Parent reported outcome measure measured as a continuous variable using pTESS (English) / TESS(English/Marathi/Hindi). 2. Gait analyses 3D gait analysis to assess movement characteristics such as joint angular kinematics, kinetics, & spatiotemporal gait parameters using a 12-camera Qualisys® 3D Motion Capture System (Qualisys AB, Götebor, Sweden). 3. Physician reported functional outcome measure as a continuous variable (MSTS, musculoskeletal tumor society scoring system) in all patientsTimepoint: Single point assessment after enrollment. | — |
Countries
India
Contacts
Public ContactDr Prakash Nayak
Tata Memorial Hospital, Mumbai
Outcome results
None listed