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NCT01596283 · ClinicalTrials.gov registry record · Phase 3

Clinical Trial of Standard Versus Goal-Directed Perioperative Fluid Management (GDT) for Patients Undergoing Liver Resection

A Phase 3 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 3
Development phase
135
Enrollment target

NCT01596283: Completed Phase 3 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01596283 is a Phase 3 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 135 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01596283, a Phase 3 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 3
Development phase
135 participants
Enrollment target

Study Summary

The purpose of this study is to help us learn what is the best amount of fluid to administer to patients during liver surgery. Patients will receive either an amount for this surgery based on weight, blood pressure, heart rate and urine output or an amount guided by a computerized system (FloTrac) that helps doctors know how much fluid each patient needs. The FloTrac calculates the amount of fluid patients needs on a minute-to-minute basis, based on real time information like blood pressure, pulse and the ability of the heart and blood vessels to maintain normal vital signs.

Interventions

  • PROCEDURE Standard fluid management
  • DEVICE Goal directed fluid therapy with the Edwards EV1000 system

Trial Details

FieldValue
Enrollment Target 135 participants
Start Date 2012-04
Est. Completion 2016-05
Phase Phase 3

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT01596283

The ClinicalTrials.gov registry entry for NCT01596283 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 135 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Standard fluid management is the first listed.

NCT01596283 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01596283 about?

NCT01596283 is a clinical study titled "Clinical Trial of Standard Versus Goal-Directed Perioperative Fluid Management (GDT) for Patients Undergoing Liver Resection". The purpose of this study is to help us learn what is the best amount of fluid to administer to patients during liver surgery. Patients will receive either an amount for this surgery based on weight, blood pressure, heart rate and urine output or an amount guided by a computerized system (FloTrac) t...

What is the current status of trial NCT01596283?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 135 participants. The study started on 2012-04. Estimated completion is 2016-05.

What interventions are being tested in trial NCT01596283?

The interventions under investigation include: Standard fluid management (PROCEDURE), Goal directed fluid therapy with the Edwards EV1000 system (DEVICE).

Who is sponsoring clinical trial NCT01596283?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.