Clinical Trials Logo

Clinical Trial Summary

Comminuted metaphyseal fractures (OTA classification A2/3 and C2/3) of the distal femur and distal tibia are difficult to treat and typically have more complications than other metaphyseal fractures. Delayed union, nonunion and need for secondary bone graft procedures are frequent outcomes. These A2/3 and C2/3 fractures of the distal femur and distal tibia treated with locked plates often have a critical sized fracture gap (poorly organized cortical pieces many of which are stripped of soft tissue). Optimal management strategies that minimize both fracture healing time and complication rates remain controversial. Primary bone grafts or early secondary bone grafts have been recommended for these comminuted open fractures, but have not been studied as the primary end point in a randomized trial. There is a need to study primary bone grafting during open reduction and internal fixation (plating) of these difficult fractures, to determine if shorter healing time, and thus less need for reoperation, can be achieved.

Hypothesis Acute autogenous bone grafting at the time of fixation will hasten clinical and radiographic union with a lower need for secondary procedures


Clinical Trial Description

Study procedures:

Eligible fractures will be identified, consented and randomized to RIA augmentation or non graft treatment. Bone graft will be harvested through the fracture at the time of the definitive fixation procedure. No additional graft can be utilized acutely (No iliac crest bone graft, or INFUSE, OP-1, Callos, etc).

Randomization Procedures: We will be using Research Randomizer to calculate a random assignment design for Group A and Group B, which will be kept by the Research Coordinator. Once a patient agrees to participate in the study and signs an Informed Consent Form, the treating surgeon will request the treatment assignment from the Research Coordinator prior to the surgery. Group A will receive RIA augmentation. Group B will receive non-graft treatment. Patient outcomes will be analyzed using intention to treat principles.

Surgical Procedures: Locked lateral plating of comminuted supracondylar femur and distal tibia fractures is an accepted standard of care. In severely comminuted fracture patterns, restoration of length and alignment often leaves substantial fracture gap increasing the risk of fracture nonunion. Historically, this has been accepted with the plan to return to the patient to surgery for bone grafting at a later date if the nonunion is developing. Intra-focal reaming with irrigation & aspiration (RIA) at time of initial surgery allows for acute autogenous bone grafting with no increased morbidity to the patient.

Surgery for Group A receiving bone graft follows the same course as without acute grafting (same incision, dissection etc.) with the exception that after initial exposure, a guide wire is placed into the proximal femoral canal (retrograde) through the fracture, and graft is harvested using the RIA system. The RIA system has a reservoir to collect the reamings as they are aspirated from the fracture site. Reduction and fixation with locked plates then proceed as usual and the harvested graft is then placed into the residual gap with the expectation that nonunion rates may be decreased. A theoretical advantage is the renewed fracture hematoma that will collect at the fracture site secondary to reaming the canal which may also increase union rates and time to union. No increased morbidity is incurred and the increased surgical time is under 10 minutes. ;


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT01553630
Study type Interventional
Source Florida Orthopaedic Institute
Contact
Status Terminated
Phase N/A
Start date May 2010
Completion date August 2014

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05459038 - Clinical Validation of the C-Arm Rotational View (CARV) to Avoid Rotational Malalignment After Intramedullary Nailing of Tibial Shaft Fractures. N/A
Terminated NCT02845245 - Comminuted Intra-Articular Distal Tibia Fracture Fixation Using Computer Techniques N/A
Completed NCT02456194 - Management of Traumatic Bone Defects in Tibial Plateau Fractures With Antibiotic-Impregnated Biodegradable Calcium Sulfate Beads: A Prospective Clinical Trial N/A
Terminated NCT00667849 - Trial to Evaluate UltraSound in the Treatment of Tibial Fractures N/A
Completed NCT01132508 - Use of a Reinforced Injectable Calcium Phosphate Bone Cement in the Treatment of Tibial Plateau Fractures N/A
Completed NCT00512434 - Percutaneous Autologous Bone-marrow Grafting for Open Tibial Shaft Fracture N/A
Completed NCT00161616 - Study Evaluating InductOs in Diaphyseal Tibia Fractures Phase 4
Terminated NCT03881241 - Safety Study of Treatment of Leg Fractures
Completed NCT02750072 - INfrapatellar Versus SUprapatellar Reamed Intramedullary Nailing for Fractures of the Tibia N/A
Completed NCT04015167 - A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the T2 Alpha Tibia Nailing System
Completed NCT05613257 - Distal Targeter vs Free-hand N/A
Completed NCT03388879 - Reamed Nailing Versus Taylor Spatial Frame in Tibia Shaft Fractures N/A
Completed NCT02491047 - Safety and Performance of BonyPid-1000™ in the Treatment of Gustilo I, II, IIIA and IIIB Tibial Open Fractures N/A
Completed NCT01797640 - Intramedullary Nailing of Tibia Fractures N/A
Recruiting NCT03232216 - Vitamin D Supplementation and Tibia Fracture. Does it Improve Healing Rate? N/A
Withdrawn NCT03826784 - Bone Healing Accelerant Versus Standard of Care for Open Tibia Fractures Phase 3
Terminated NCT00253981 - Light Therapy in the Treatment of Leg Pain N/A
Completed NCT05303389 - Posterior Plating Versus Anterior to Posterior Screws in Fixation of Posterior Column in Pilon Fractures N/A
Recruiting NCT05272631 - Depuy Synthes Lower Extremity Shaft Nail Registry
Completed NCT03540719 - Surgical Management of Posterior Tibial Plateau Fractures