Proximal Femoral Fracture Clinical Trial
Official title:
Can a Multimodal Approach Improve the Outcome of Patients With a Proximal Femoral Fracture?
This study is designed to compare the outcome of patients with proximal femoral fractures with different perioperative regimes: a group with a multimodal intervention and a control group.
Femoral neck fractures constitute both a social and economic challenge. The one year
mortality of affected patients amounts to 33%, wherein cardio-vascular complications are the
major contributor. It is an objective of the present study to investigate whether a
multi-modal perioperative intervention can improve the outcome of these patients.
We plan to carry out a prospective randomized controlled clinical study. Patients with an age
above 60 years and proximal femoral fractures (femoral neck fractures or pertrochanteric
femoral fractures) are to be included. These are divided into two groups, K and M. General
anaesthesia is applied to both groups. In group K a commonly used therapy will be applied
whereas in group M an intesified perioperative care will be carried out. The objectives are
to provide sufficient analgesia, normotonia and normothermia. Hence, a femoral catheter is
applied for pain therapy already preoperatively. Moreover, the pulmonal situation is improved
by means of oxygen as needed. The cardiovascular situation is evaluated and optimized by
means of extended hemodynamic monitoring both pre- and postoperatively. If needed, the
nutrition of the patients is supplemented with highly caloric drinks.
A primary common endpoint is the appearance of postoperative complications. These include
cardiovascular, cerebrovascular, pulmonal, renal and surgical complications. Secondary
endpoints are mortality, duration of the stay at the hospital and intensive care duration. It
is the objective of the study to reduce the probability for at least one postoperative
complication from 50% to 25% (α=0,05 and 1-β=0,80). To this end 132 patients would have to be
included in the study.
All participants are to be contacted by phone one year after the surgery and their health
situation is to be determined.
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