Clinical Trials Directory

Trials / Completed

CompletedNCT01673776

Multimodal Approach to Improve the Outcome of Patients With a Proximal Femoral Fracture

Can a Multimodal Approach Improve the Outcome of Patients With a Proximal Femoral Fracture?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
132 (actual)
Sponsor
Technical University of Munich · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DEVICEPulsioFlex® Monitoring* goal directed therapy according to PulsioFlex® Monitoring- measurements * femoral catheter * extended perioperative monitoring * nutritional supplementation, (if necessary)

Timeline

Start date
2012-03-01
Primary completion
2016-10-01
Completion
2016-10-15
First posted
2012-08-28
Last updated
2018-08-08

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01673776. Inclusion in this directory is not an endorsement.