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NCT Number: NCT07444593

Transverse Tibial Bone Transport (TTT) in the Management of Chronic Diabetic Lower Extremity Wounds

The purpose of this study is to evaluate the safety and clinical performance of transverse tibial bone transport in patients with chronic ischemic and diabetic lower extremity ulcers. This study will assess wound healing outcomes and limb preservation in a population with limited therapeutic alternatives.

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Key information

Age range

22 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic

Jacksonville, Florida, 32224, United States

Location contact

Bre Jenkins

CONTACT

[email protected]

Elizabeth Wellings, MD

PRINCIPAL_INVESTIGATOR

Lauren Evans

CONTACT

[email protected]

904-953-5416

Thea Price, MD

SUB_INVESTIGATOR

About this study

Diabetic lower extremity ulcers are associated with impaired blood flow, delayed wound healing, high morbidity, and an increased risk of limb loss. In some patients, conventional treatments such as wound care, revascularization procedures, or adjunctive therapies are ineffective or not feasible, leaving limited options short of major amputation.

Transverse tibial bone transport (TTT) is a surgical technique that applies controlled distraction to the tibial cortex and has been reported in prior clinical studies to stimulate angiogenesis, improve local perfusion, and support wound healing in ischemic conditions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (>=22 years).
  • Chronic diabetic foot ulcer wound persisting >=12 weeks and less than 104 weeks refractory to standard wound care.
  • Wound location within distal 1/3 tibia and below including foot.
  • Wound stages: WiFi >= 3
  • At least one patent lower extremity tibial vessel (after revascularization if needed).
  • Able to provide informed consent and comply with study procedures.

Exclusion criteria

  • Active systemic infection (positive blood cultures)
  • Severe sepsis (2 out of 4 SIRS criteria with impact on organ dysfunction)
  • Subacute lower extremity wound <12 weeks with or without standard wound cares
  • Internal hardware within 10cm of possible TTT placement
  • Most proximal aspect of wound within 10cm of most distal pin of possible TTT placement
  • End Stage Renal Disease requiring dialysis
  • Renal function values
  • eGFR: <15ml/min and
  • Creatinine: >6mg/dL and
  • BUN: >50 mg/dL
  • Wounds less than 1 cm3 or greater than 30 cm3
  • Corticosteroids >10mg prednisone equivalent daily for >2 weeks
  • Patients with osteomyelitis in the ipsilateral tibia at planned corticotomy site
  • Cognitive or social limitations precluding consent or follow-up
  • Current participation in another investigational study (drug or device)
  • Immunocompromised (WBC <4) or undergoing active chemotherapy
  • Hemoglobin A1c >12
  • BMI <18.5 kg/m2
  • Pregnant, lactating, or planning to become pregnant
  • Life expectancy less than 12 months
  • Severe hepatic impairment defined by patient on a transplant list, MELD > 20, Child's class C.
  • A history of conditions that may impair wound healing in the opinion of the Investigator, for example, autoimmune disorders, renal failure patients on dialysis, or medications that impair the healing process.

Treatment and study plan

Biodynamik XT3

Device

Application of XT3 system and transverse tibial bone transport procedure

Primary outcomes

  1. Proportion of subjects with wound closure

    Time frame: From enrollment to 18 weeks

    To demonstrate the safety and effectiveness of the investigational procedure, when used in addition to standard wound care, in promoting clinically meaningful healing of chronic diabetic foot ulcers, specifically, to demonstrate that the proportion of subjects with wound closure is greater for the investigational procedure than standard wound care alone at 18 weeks while maintaining an acceptable safety profile. Proportion of subjects with wound closure as defined as 100% re-epithelialization of the target diabetic foot ulcer where there is no drainage or dressing is not required and confirmed at two consecutive study visits 2 weeks apart.

Secondary outcomes

  1. Mean PAR summarized at 8 and 18 weeks

    Time frame: From enrollment to 18 weeks

    To compare mean Percent Area Reduction (PAR) between treatment groups at 8 and 18 weeks

  2. Proportion of patients with greater than 60% PAR

    Time frame: From enrollment until 18 weeks

    To compare the proportion of patients with PAR of greater than 60% at 8 and 18 weeks..

  3. Frequency of subsequent procedures

    Time frame: From enrollment to 18 weeks

    Frequency of subsequent procedures (surgical debridement; minor/major amputation)

  4. Vascular changes as measured by Ankle Brachial Index (ABI)

    Time frame: From enrollment to 18 weeks, 6, 9 and 12 months

    ABI (No units; ratio) at 18 weeks and at 6, 9 and 12 months

  5. Improvement in Visual Analog Scale to measure pain

    Time frame: From enrollment to 18 weeks

    Improvement in pain as measured in a 10 point Visual Analogue Scale (VAS) at 8 and 18 weeks. VAS lowest score is 0 (no pain). While 10 is the highest score (worst pain).

  6. Frequency of wound recurrence

    Time frame: Enrollment until 12 months

    Frequency of wound recurrence/re-ulceration at 12 weeks and at 6, 9 and 12 months

  7. Amputation free survival

    Time frame: Enrollment until 12 months

    Amputation free survival at 12 weeks and at 6, 9 and 12 months

  8. Vascular changes as measured by Transcutaneous Oxygen Pressure (TcPO2)

    Time frame: Measured at baseline to 18 weeks and through 12 months

    TcPO2 (mmHG) at 6 weeks, 18 weeks and at 6, 9 and 12 months. Oxygen tension at the skin surface, reflecting tissue oxygenation and perfusion.

  9. Improvement in Patient Reported Outcome Wound-QoL-17 at 16 weeks

    Time frame: From enrollment to 18 weeks

    Improvement in Quality of Life Measure Wound-QoL-17 at 18 weeks. Score (0-4 mean or 0-68 total; Transformed score 0-100

  10. Time to achieve wound closure

    Time frame: Enrollment through 18 weeks and 12 months

    Compare the time to achieve wound closure at 18 weeks and through 12 months

  11. Time to heal for surgical site

    Time frame: Enrollment to 18 weeks

    Time to heal for pin sites, incision sites and bone consolidation

Other outcomes

  1. Safety Endpoint - Adverse Events

    Time frame: Enrollment to 18 weeks

    • Frequency of treatment-emergent serious and non-serious adverse events
  2. Safety endpoint - TTT Related

    Time frame: Enrollment to 18 weeks

    Frequency of device-related adverse events in the TTT arm including pin site infection and device breakage

  3. Plasma growth factor level changes as measured by VEGf at 18 weeks and at 6,9 and 12 months

    Time frame: From enrollment until 12 months

    Vascular Endothelial Growth Factor) measured in either picograms per milliliter (pg/mL) or nanograms per liter (ng/L) in serum or plasma

  4. Vascular Perfusion measured by Computed Tomography Angiogram (CTA) at 18 weeks and at 6, 9 and 12 months

    Time frame: Through 12 months

    CTA is measured in Hounsfield Units (HU)

Study contacts

Contact information is provided by the study sponsor or research team.

Elizabeth Wellings, MD

CONTACT

[email protected]

9049532496

Lauren Evans

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Biodynamik, Inc

Industry

Collaborators

  • Mayo Clinic

Registry information

Official study title

SMILE - TTT: Surgical MIcrovascularization of Lower Extremities for Diabetic Foot Ulcers - Transverse Tibial Transport Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Mar 3, 2026
Registry last updated
Apr 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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