← Eichor
Study identifier: NCT06156384 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Assess the Pain, Satisfaction, and Quality of Life of Patients With FITBONE® Lengthening Nail

Condition: Leg Length Inequality  ·  Sponsor: Orthofix s.r.l.

PhaseN/A
Planned participants45
Who can joinAll sexes, 12 Years to no upper limit
Healthy volunteersNo

About this study

This study is a prospective observational non-interventional multi-centre cohort study of patients, 12 years or older, initiating a lower limb lengthening procedure with FITBONE and who have a length discrepancy of 30mm or more between the limbs. The following parameters will be assessed for up to 24 months. * Pain using the Visual Analog Scale (VAS), Patient Global Assessment (PGA) and Clinical Observer Global Assessment (COGA) * Patient satisfaction using the Patient Global Impression of change (PGI-C) scale * QoL using the 36-Item Short Form Survey/Paediatric Quality of Life Inventory (SF-36/PedsQL)

This description comes directly from the study's public registry record.

Talk to the study team

Tommaso Marano  ·  +39 0456719000  ·  tommasomarano@orthofix.it

Daniela Cangiano  ·  +39 0456719000  ·  danielacangiano@orthofix.it

Always discuss trial participation with your own doctor first.

Locations (6)

CHU de Saint-Étienne Hôpital NordSaint-Etienne, Auvergne-Rhône-Alpes, FranceRecruiting
CHU de StrasbourgStrasbourg, Grand Est, FranceRecruiting
CHU Lille - Hôpital Jeanne de FlandreLille, Hauts-de-France, FranceRecruiting
Centre hospitalier universitaire (CHU) de ToulouseToulouse, Occitanie, FranceRecruiting
Hôpital Sainte-Marguerite AP-HMMarseille, Provence-Alpes-Côte d'Azur Region, FranceRecruiting
CHU de La Réunion site Sud Saint-PierreSaint-Pierre, La Réunion, ReunionRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06156384