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Stroke Volume Optimisation in Patients With Hip Fracture

NCT00444262 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 215

Last updated 2011-10-07

No results posted yet for this study

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.

Conditions

  • Hip Fractures

Interventions

PROCEDURE

hemodynamic optimisation guided using esophageal Doppler

hemodynamic optimisation guided using esophageal Doppler

DRUG

VOLUVEN and others solute

VOLUVEN and others solute

Sponsors & Collaborators

  • Fresenius Kabi

    collaborator INDUSTRY

  • GAMIDA

    collaborator UNKNOWN

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • bernard CHOLLEY, MD PhD · Assistance Publique - Hôpitaux de Paris

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-04-30
Primary Completion
2010-11-30
Completion
2011-03-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00444262 on ClinicalTrials.gov