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NCT01244685 · ClinicalTrials.gov registry record · NA

Trial With Deltex Cardio in Elective Bowel Resection Patients

A NA study of 1 Fluid Management, sponsored by Stony Brook University.

Completed
Registry status
NA
Development phase
58
Enrollment target
1
Study location

NCT01244685 is a NA study of 1 Fluid Management that has completed, run by Stony Brook University. The registered enrollment target is 58 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT01244685, a NA study of 1 Fluid Management, has completed, sponsored by Stony Brook University.

COMPLETED
Registry status
NA
Development phase
58 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is: * To determine if the intraoperative fluid administration with the Deltex CardioQ esophageal Doppler will reduce the length of stay after elective bowel resection. * The probe can be used to dynamically measure stroke volume and cardiac output. This information will assist us in determining the ideal amount of fluids to be administered. * To determine if the fluid administration established by the esophageal probe will result in a shorter length of stay in elective bowel resection patients. * The investigators plan to enroll 100 patients in this study.

Conditions Studied

Interventions

  • DEVICE Deltex CardioQ Probe

Study Locations (1)

New York

  • Stony Broook University Medical Center - Stony Brook

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2010-03
Est. Completion 2011-11
Phase NA

Sponsor

Stony Brook University

127 total trials

What the Registry Record Tells You About NCT01244685

The ClinicalTrials.gov registry entry for NCT01244685 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 58 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stony Brook University, which has 127 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with 1 Fluid Management appearing as the primary indexed condition, and to 1 intervention - of which Deltex CardioQ Probe is the first listed.

NCT01244685 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01244685 about?

NCT01244685 is a clinical study titled "Trial With Deltex Cardio in Elective Bowel Resection Patients". The purpose of this study is: * To determine if the intraoperative fluid administration with the Deltex CardioQ esophageal Doppler will reduce the length of stay after elective bowel resection. * The probe can be used to dynamically measure stroke volume and cardiac output. This information will as...

What is the current status of trial NCT01244685?

This trial is currently completed. It is a NA study. The enrollment target is 58 participants. The study started on 2010-03. Estimated completion is 2011-11.

What conditions does trial NCT01244685 study?

This clinical trial studies the following conditions: 1 Fluid Management.

What interventions are being tested in trial NCT01244685?

The interventions under investigation include: Deltex CardioQ Probe (DEVICE).

Who is sponsoring clinical trial NCT01244685?

This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01244685 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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, or report a data error.