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Clinical Trials/EUCTR2011-000254-39-SE
EUCTR2011-000254-39-SE
Active, Not Recruiting
Phase 1

Perioperative Goal Directed Fluid Therapy during Esophageal Resection. A prospective randomized controlled open multi-centre trial to study the effect on postoperative complications

Anestesi och Operationskliniken0 sites65 target enrollmentJuly 18, 2011
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ConditionsAnesthesia for esophageal resection because of malignancyTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsVolulyte

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Anesthesia for esophageal resection because of malignancy
Sponsor
Anestesi och Operationskliniken
Enrollment
65
Status
Active, Not Recruiting
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 18, 2011
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Anestesi och Operationskliniken

Eligibility Criteria

Inclusion Criteria

  • •Patients scheduled for elective esophageal resection because of malignancy without colon interposition
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range 30
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range 35

Exclusion Criteria

  • •\- ASA\-class 4 or higher
  • •\- Signifikant aortic/mitral insufficiency
  • •\- Extensive hemodynamic monitoring planned excluding Invasive Arterial Blood Pressure, ElectroCardioGraphy, Central Venous Pressure and diuresis
  • •\- Contraindikations to artificila kolloids such as allergy, severe kidney/liverdisease or severe hypernatremia

Outcomes

Primary Outcomes

Not specified

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