Clinical Validation of the C-Arm Rotational View (CARV) to Avoid Rotational Malalignment After Intramedullary Nailing of Tibial Shaft Fractures.
Tibial Fractures, Surgery, Complication,Postoperative
About this trial
This is an interventional supportive care trial for Tibial Fractures focused on measuring Intramedullary nailing, Tibia shaft fractures, Rotational malalignment, C-Arm Rotational View, multi-center randomized controlled trial.
Eligibility Criteria
Inclusion Criteria:
- All consecutive patients (≥18 years) with an open or closed tibia shaft fracture, who are eligible for IMN, will be asked to enroll in the study
Exclusion Criteria:
- The following exclusion criteria will be used: age <18 years, fractures not suitable for IMN and pathological fractures.
Sites / Locations
- Flinders Medical Centre, Flinders University
- University Medical Centers Groningen
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Interventional group
Control group
Patients assigned to the interventional group will undergo an identical surgical procedure as patients assigned to the control group. The only difference with the control group is that tibial alignment will be obtained according to the standardized CARV-protocol.
Patients assigned to the control group will undergo an identical surgical procedure as patients assigned to the interventional group. The only difference with the intervention group is that tibial alignment will be obtained according to present unstandardized clinical standards