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Stroke Volume Optimisation in Patients With Hip Fracture (FRACTALE)

Primary Purpose

Hip Fractures

Status
Terminated
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
hemodynamic optimisation guided using esophageal Doppler
VOLUVEN and others solute
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hip Fractures focused on measuring Hemodynamic optimisation, Esophageal Doppler, Hydroxy ethyl starch, Hip fracture, Outcome, Elderly subjects (≥ 70 year old), General anesthesia

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Centre Hospitalier Universitaire de La Cote de Nacre
  • Hopital Purpan
  • Hopital Antoine Beclere
  • Hopital D'Instruction Des Armees Percy
  • Hopital Beaujon
  • Hopital Lapeyronie
  • Centre Hospitalier de Meaux
  • Centre Hospitalier Universitaire Rouen
  • Hopital Avicenne
  • Hopital Henri Mondor
  • Hopital Bicetre
  • Centre Hospitalier Universitaire de Poitiers
  • Hopital Lariboisiere
  • Hopital Saint Antoine
  • Hopital La Pitie Salpetriere
  • Fondation Saint Joseph
  • Hopital Cochin
  • Hopital Europeen Georges Pompidou
  • Hopital Bichat

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

1

2

Arm Description

conventional treatment

stroke volume optimisation

Outcomes

Primary Outcome Measures

We expect a 30% reduction in the number of per- and post-operative complications observed during hospitalisation in acute care beds in the "optimised" subgroup with respect to "conventional" subgroup. Complications include: death, per-operative

Secondary Outcome Measures

We will check if patients in the "optimised" group have:1) a reduction in the delay to walk without help2) more days " out-of-hospital " at 3 months 3) a reduction in 1-year mortality rate

Full Information

First Posted
March 6, 2007
Last Updated
October 6, 2011
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fresenius Kabi, GAMIDA
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1. Study Identification

Unique Protocol Identification Number
NCT00444262
Brief Title
Stroke Volume Optimisation in Patients With Hip Fracture
Acronym
FRACTALE
Official Title
Study Multicentric, Randomised, in Duplicate Blind Person of the Impact of a Per Operatory Strategy of Optimization of the Cardiac Output on the Forecast of the Old Subjects Operated for Fracture of the Upper End of the Femur " FRACTALE "
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Terminated
Why Stopped
termination of the study due to difficulties to include patients
Study Start Date
April 2007 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fresenius Kabi, GAMIDA

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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 fracture.
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 increased mortality. Perioperative tissue hypoperfusion may participate in the development of postoperative complications. Hypovolemia is secondary to many factors in hip fracture patients (including blood loss, fasting and dehydration) and can result in low cardiac output and tissue hypoperfusion. Two single-center, randomized, double-blind studies have demonstrated that peroperative fluid titration guided by esophageal Doppler measurements of stroke volume could improve patient outcome. Interpretation of these results was that such a stroke volume "optimisation" strategy could help the anesthesiologist give more fluids to his patient and reduce the risk of hypoperfusion without the risk of congestion, thereby reducing postoperative complications and improving patient outcome. We want to test the same hypothesis in a multicenter trial to confirm with a high level of proof the usefulness of this strategy. If previous results are confirmed, this could lead to a change in current anesthetic management of hip fracture patients and potentially have a very important economical impact on health costs.Goals : Primary endpoint is to demonstrate that colloid (Voluven®) titration, guided using esophageal Doppler estimation of stroke volume, during the surgical repair of hip fracture reduces the incidence of postoperative complications (composite criteria). Secondary endpoints in the "optimised group" include : 1) reduced delay to walk without help ; 2) increased number of days " out-of-hospital " at 3 months after the fracture ; and 3) reduced 1-year mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fractures
Keywords
Hemodynamic optimisation, Esophageal Doppler, Hydroxy ethyl starch, Hip fracture, Outcome, Elderly subjects (≥ 70 year old), General anesthesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
215 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
conventional treatment
Arm Title
2
Arm Type
Experimental
Arm Description
stroke volume optimisation
Intervention Type
Procedure
Intervention Name(s)
hemodynamic optimisation guided using esophageal Doppler
Intervention Description
hemodynamic optimisation guided using esophageal Doppler
Intervention Type
Drug
Intervention Name(s)
VOLUVEN and others solute
Intervention Description
VOLUVEN and others solute
Primary Outcome Measure Information:
Title
We expect a 30% reduction in the number of per- and post-operative complications observed during hospitalisation in acute care beds in the "optimised" subgroup with respect to "conventional" subgroup. Complications include: death, per-operative
Time Frame
during hospitalisation in acute care
Secondary Outcome Measure Information:
Title
We will check if patients in the "optimised" group have:1) a reduction in the delay to walk without help2) more days " out-of-hospital " at 3 months 3) a reduction in 1-year mortality rate
Time Frame
at 3 months and at one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
bernard CHOLLEY, MD PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier Universitaire de La Cote de Nacre
City
Caen
State/Province
Calvados
ZIP/Postal Code
14000
Country
France
Facility Name
Hopital Purpan
City
Toulouse
State/Province
Haute Garonne
ZIP/Postal Code
31000
Country
France
Facility Name
Hopital Antoine Beclere
City
Clamart
State/Province
Hauts de Seine
ZIP/Postal Code
92140
Country
France
Facility Name
Hopital D'Instruction Des Armees Percy
City
Clamart
State/Province
Hauts de Seine
ZIP/Postal Code
92140
Country
France
Facility Name
Hopital Beaujon
City
Clichy
State/Province
Hauts de Seine
ZIP/Postal Code
92110
Country
France
Facility Name
Hopital Lapeyronie
City
Montpellier
State/Province
Herault
ZIP/Postal Code
34000
Country
France
Facility Name
Centre Hospitalier de Meaux
City
Meaux
State/Province
Seine Et Marne
ZIP/Postal Code
77100
Country
France
Facility Name
Centre Hospitalier Universitaire Rouen
City
Rouen
State/Province
Seine Maritime
ZIP/Postal Code
76000
Country
France
Facility Name
Hopital Avicenne
City
Bobigny
State/Province
Seine Saint Denis
ZIP/Postal Code
93009
Country
France
Facility Name
Hopital Henri Mondor
City
Creteil
State/Province
Val de Marne
ZIP/Postal Code
94000
Country
France
Facility Name
Hopital Bicetre
City
Le Kremlin Bicetre
State/Province
Val de Marne
ZIP/Postal Code
94275
Country
France
Facility Name
Centre Hospitalier Universitaire de Poitiers
City
Poitiers
State/Province
Vienne
ZIP/Postal Code
86000
Country
France
Facility Name
Hopital Lariboisiere
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Hopital Saint Antoine
City
Paris
ZIP/Postal Code
75012
Country
France
Facility Name
Hopital La Pitie Salpetriere
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Fondation Saint Joseph
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Hopital Cochin
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Hopital Europeen Georges Pompidou
City
Paris
ZIP/Postal Code
75015
Country
France
Facility Name
Hopital Bichat
City
Paris
ZIP/Postal Code
75018
Country
France

12. IPD Sharing Statement

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Stroke Volume Optimisation in Patients With Hip Fracture

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