Status:
TERMINATED
Stroke Volume Optimisation in Patients With Hip Fracture
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Collaborating Sponsors:
Fresenius Kabi
GAMIDA
Conditions:
Hip Fractures
Eligibility:
All Genders
70+ years
Phase:
PHASE3
Brief Summary
The aim of this study is to assess whether intra-operative fluid supplementation (to improve tissue perfusion) can reduce the incidence of postoperative complications in elderly patients with hip frac...
Detailed Description
Rationale : Hip fracture patients frequently develop postoperative complications that increase their hospital length of stay and the cost of care. These complications are also associated with increase...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Elderly subjects (≥ 70 year old) with hip fracture
- Exclusion criteria:
- Patient or legal representative unwilling to give informed consent
- Patient with other trauma lesions associated to hip fracture
- Patient with esophageal disease or chronic dissection of the descending aorta (contra-indications to esophageal Doppler monitoring)
- Patient with known active neoplasia or with obvious metastatic hip fracture
- Allergy to hydroxy-ethyl starches
- Congenital hemostatic disorder
Exclusion
Key Trial Info
Start Date :
April 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2011
Estimated Enrollment :
215 Patients enrolled
Trial Details
Trial ID
NCT00444262
Start Date
April 1 2007
End Date
March 1 2011
Last Update
October 7 2011
Active Locations (19)
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1
Centre Hospitalier Universitaire de La Cote de Nacre
Caen, Calvados, France, 14000
2
Hopital Purpan
Toulouse, Haute Garonne, France, 31000
3
Hopital Antoine Beclere
Clamart, Hauts de Seine, France, 92140
4
Hopital D'Instruction Des Armees Percy
Clamart, Hauts de Seine, France, 92140