Mayo Clinic
Jacksonville, Florida, 32224, United States
Location contact
Bre Jenkins
CONTACT
Elizabeth Wellings, MD
PRINCIPAL_INVESTIGATOR
Lauren Evans
CONTACT
Thea Price, MD
SUB_INVESTIGATOR
NCT Number: NCT07444593
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.
Trial opening soon.
Get Notified22 year and older
All sexes
Interventional
Not applicable
Jacksonville, Florida, 32224, United States
Bre Jenkins
CONTACT
Elizabeth Wellings, MD
PRINCIPAL_INVESTIGATOR
Lauren Evans
CONTACT
Thea Price, MD
SUB_INVESTIGATOR
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Application of XT3 system and transverse tibial bone transport procedure
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.
Time frame: From enrollment to 18 weeks
To compare mean Percent Area Reduction (PAR) between treatment groups at 8 and 18 weeks
Time frame: From enrollment until 18 weeks
To compare the proportion of patients with PAR of greater than 60% at 8 and 18 weeks..
Time frame: From enrollment to 18 weeks
Frequency of subsequent procedures (surgical debridement; minor/major amputation)
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
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).
Time frame: Enrollment until 12 months
Frequency of wound recurrence/re-ulceration at 12 weeks and at 6, 9 and 12 months
Time frame: Enrollment until 12 months
Amputation free survival at 12 weeks and at 6, 9 and 12 months
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.
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
Time frame: Enrollment through 18 weeks and 12 months
Compare the time to achieve wound closure at 18 weeks and through 12 months
Time frame: Enrollment to 18 weeks
Time to heal for pin sites, incision sites and bone consolidation
Time frame: Enrollment to 18 weeks
Time frame: Enrollment to 18 weeks
Frequency of device-related adverse events in the TTT arm including pin site infection and device breakage
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
Time frame: Through 12 months
CTA is measured in Hounsfield Units (HU)
Contact information is provided by the study sponsor or research team.
Biodynamik, Inc
Industry
SMILE - TTT: Surgical MIcrovascularization of Lower Extremities for Diabetic Foot Ulcers - Transverse Tibial Transport Study
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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