Clinical Trial Search

Primary: Number of Participants With a Superficial Incisional Surgical Site Infection (SSI) — 13; 7 Participants

Primary: Healing of Orthopaedic Trauma Open Fractures — 3.2; 4.0 use days

Primary: Constant Scale Evaluation at 3 Months and 12 Months From the Date of Trauma — 40.1; 51.8 units on a scale — p=<0.01

Primary: Average Difference Between Michigan Hand Outcomes Questionnaire Scores — 85.2; 91.8 units on a scale

Primary: Incidence of Surgical Site Infection During the Post-operative Follow-up Period — 0; 0; 0 participants

Primary: Time of Union — 5.8 weeks

Primary: Incidence of Surgical Site Infection (SSI) Relating to Intramedullary Nailing for Fixation of Diaphyseal Femoral and Tibial Fractures — 26; 195 Participants

Primary: The Number of Participants With Re-operations (All Subsequent Operative Procedures to Treat an Infection, a Wound Healing Problem, or a Nonunion). — 7; 6; 3; 10…

Primary: Loss of Radius Fracture Reduction — 35; 35; 66; 66 participants — p=1.00

Primary: Radiologic Evidence of Bone Healing — 12.6; 11.2; 15.4; 13.2 units on a scale

Primary: Time to Distal Femur Fracture Healing by Radiographic Evidence — 1.75; 2.15 months

Primary: EQ-5D — 69.23; 72.81; 74.24; 73.04 units on a scale

Primary: Participants' Quality of Life at 3 Months — 0.60; 0.59 score on a scale

Primary: Fracture Union — 27; 2 participants

Primary: Difference in the Two Groups in Regards to Resident Time. — 24; 57 minutes

Primary: Number of Participants With Tissue Samples Identified With Bacterial DNA According to Highly Sensitive Bacterial Assays — 10; 24; 20 Participants

Primary: Number of Participants With a Superficial Incisional Surgical Site Infection (SSI) — 20; 27; 6; 9 Participants

Primary: Number of Patients With Healed Fractures — 83; 66; 8; 13 patients — p=0.0541

Primary: Sensitivity — 96.7 percent of scans with a fracture

Primary: The Grip Strength — 98.3; 62.6 Percentage of opposite side — p=<0.05

Primary: Number of Participants With Total Wound Infections — 4; 9 participants — p==0.12

Primary: Percent of Patients That Complete the Protocol — 61.5; 83.3; 0 percentage of completed patients

Primary: Pain Levels on a Visual Analog Scale ( VAS) — 7.05; 4.03; 7.49; 6.60 units on a scale — p=<0.10

Primary: Percentage of Responders at 6 Months (Efficacy of ALLOB) — 100 percent of patients

Primary: Effectiveness Will be Measured for AMERICAN SHOULDER AND ELBOW (ASES) Score — 66; 77 score on a scale — p=0.048

Primary: Percentage of Nonpalpable Hardware — 71; 55; 64; 66 percentage of participants

Primary: Posttreatment Pain — 5.3; 6.2; 4.2; 5.6 scores on a scale

Primary: Resorption of Study Device — 4 Participants

Primary: Time to Place Archbars — 14.07; 37.29 minutes

Primary: Duration of Time the Patient Was in the OR as a Measure of Effectiveness of the Treatment — 107.0 Minutes