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NCT01397331

Influence of Anesthesia on Mechanical Efficiency of Left Ventricle in Patients Undergoing Open Heart Surgery

Terminated Phase 4 Last updated 24 April 2018
What this trial tests

Phase 4 trial testing Isoflurane in Heart; Dysfunction Postoperative, Cardiac Surgery in 28 participants. Terminated before completion.

Timeline
1 July 2010
Primary endpoint
27 June 2012
27 June 2012

Quick facts

Lead sponsorSheba Medical Center
PhasePhase 4
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment28
Start date1 July 2010
Primary completion27 June 2012
Estimated completion27 June 2012
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Sheba Medical Center

Who can join

18 and older, any sex, with Heart; Dysfunction Postoperative, Cardiac Surgery or Disorder; Heart, Functional, Postoperative, Cardiac Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to delineate and compare the changes in coupled mechanical properties of left ventricle and arterial vascular bed caused by two popular anesthetic protocols commonly used in cardiac surgery (intravenous, based on the infusion of propofol, versus inhalational, based on isoflurane) on different stages of the surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Isoflurane

Trials testing the same drug.

Other Sheba Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01397331.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing