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The TrueLok Elevate Transverse Bone Transport System is a modular external fixation device designed for transverse bone transport. It promotes local vascular and wound healing through controlled corticotomy and gradual distraction. The system is intended for adult patients with bony and/or soft tissuedefects.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Transverse Bone Transport System | Device | This is a prospective, international, multicentre, observational post-market clinical follow-up (PMCF) study. Adult subjects will be treated according to the manufacturer's Instructions for Use, with follow-up extending to 12 months post-device removal. Participating sites include centres in the US, Europe, the UK, and South Africa. Subjects will be followed using a phased framework: T0: Index Surgery (baseline data, operative details, ulcer status) T1: End of Distraction (device parameters, adverse events, ulcer status) T2: End of Compression (similar to T1) T3: Device Removal (confirmation of union, ulcer status) Post-removal visits: F3: 3 months F6: 6 months F12: 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Complete ulcer healing | Proportion of subjects achieving complete ulcer healing within 12 months of device removal. Healing is defined as full epithelialisation with no open wound. | 12 months |
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Inclusion Criteria:
Aged 18 years or older at the time of surgery Willing and able to sign and date the study-specific informed consent form in accordance with national and institutional ethics requirements Willing and able to comply with requirements of the protocol, including follow-up requirements Indicated for surgical intervention using the TrueLok Elevate Transverse Bone Transport System for the treatment of soft tissue defects in the form of lower limb ulcers
Presence of a chronic ulcer, defined as:
Exclusion Criteria:
Mental or cognitive impairment or physiological or behavioural conditions that, in the opinion of the investigator, would preclude reliable adherence to postoperative care instructions, follow-up assessments, or study procedures
Known or presenting with the following signs of a systemic inflammatory response syndrome (SIRS) as exhibiting two or more of the following conditions:
o
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Patients affected by chronic foot ulcers
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jay Erturan, MD | Contact | 7779 32 32 44 | +44 | jerturan@orthofix.co.uk |
| Daniela Cangiano, PhD | Contact | 0456719000 | +39 | danielacangiano@orthofix.it |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Helios Klinikum Wuppertal GmbH | Recruiting | Wuppertal | Germany |
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| ID | Term |
|---|---|
| D014456 | Ulcer |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| General Regional Hospital F. Miulli of Acquaviva delle Fonti | Recruiting | Acquaviva delle Fonti | Bari | Italy |
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| Stellenbosch University | Recruiting | Cape Town | Western Cape | 7505 | South Africa |
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| Hospital de la Santa Creu i Sant Pau | Recruiting | Barcelona | 08041 | Spain |
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| Hull University Teaching Hospitals NHS Trust | Recruiting | Hull | Hull | United Kingdom |
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