TrueLok Elevate PMCF Study

NCT07079774 | Recruiting

• 1 other identifier: CIP-TLEL-25
• Study Type: observational
• Target: 153
• Locations: 5 countries
• Sites: 5

Brief Summary

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.

Conditions

Wound of Skin; Ulcers; Soft Tissue Defect

Outcome Measures

Primary Outcomes (1)

• 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

Interventions

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

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients affected by chronic foot ulcers

You may qualify if:

• 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:
• Present for at least 3 months, and
• Unresponsive to standard non-surgical or surgical wound management, including but not limited to debridement, negative pressure wound therapy (VAC), offloading, antibiotics, or vascular optimisation

You may not qualify if:

• 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:
• Heart rate \>90 beats/min
• Respiratory rate \>20 breaths/min
• PaCO2 \<32-mm Hg
• White blood cell count \>12.000 or \<4.000/cu mm
• % immature (band) forms Known hypersensitivity or allergy to any material used in the TrueLok Elevate Transverse Bone Transport System (e.g., stainless steel, titanium) Current participation in another interventional clinical study that, in the opinion of the investigator, may interfere with the objectives or outcomes of this study Presence of active malignancy or systemic infection that, in the investigator's opinion, may interfere with wound healing or the study protocol Life expectancy of less than 12 months Simultaneous bilateral application of the TrueLok Elevate Transverse Bone Transport System Current incarceration at the time of enrolment Any condition or clinical circumstance that, in the opinion of the investigator, would make participation not in the best interest of the subject or would interfere with the study objectives

Sponsors & Collaborators

• Orthofix s.r.l.: lead

Study Sites (5)

Helios Klinikum Wuppertal GmbH

Wuppertal, Germany

RECRUITING

General Regional Hospital F. Miulli of Acquaviva delle Fonti

Acquaviva delle Fonti, Bari, Italy

RECRUITING

Stellenbosch University

Cape Town, Western Cape, 7505, South Africa

RECRUITING

Hospital de la Santa Creu i Sant Pau

Barcelona, 08041, Spain

RECRUITING

Hull University Teaching Hospitals NHS Trust

Hull, Hull, United Kingdom

RECRUITING

MeSH Terms

Conditions

Ulcer

Condition Hierarchy (Ancestors)

Pathologic Processes; Pathological Conditions, Signs and Symptoms

Central Study Contacts

Jay Erturan, MD

CONTACT

7779 32 32 44; jerturan@orthofix.co.uk

Daniela Cangiano, PhD

CONTACT

0456719000; danielacangiano@orthofix.it

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 3, 2025
• First Posted: July 23, 2025
• Study Start: November 24, 2025
• Primary Completion (Estimated): November 24, 2028
• Study Completion (Estimated): November 24, 2028
• Last Updated: April 1, 2026

Record last verified: 2026-03

Locations

ES (1); GB (1); IT (1); ZA (1); DE (1)