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NCT03054922 · ClinicalTrials.gov registry record · Phase 3

Impact of Intraoperative Fluid Management on Electrolyte and Acid-base Variables

A Phase 3 study of Anesthesia, sponsored by Nationwide Children's Hospital.

Completed
Registry status
Phase 3
Development phase
59
Enrollment target
1
Study location

NCT03054922 is a Phase 3 study of Anesthesia that has completed, run by Nationwide Children's Hospital. The registered enrollment target is 59 participants, below the 109,409-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03054922, a Phase 3 study of Anesthesia, has completed, sponsored by Nationwide Children's Hospital.

COMPLETED
Registry status
Phase 3
Development phase
59 participants
Enrollment target
1
Study location

Study Summary

During major surgical procedures, intravascular volume is maintained with the administration of isotonic fluids such as Lactated Ringers (LR), Normal Saline (NS) or Normosol-R. All three of these fluids are in common clinical use for this purpose. As large volumes of NS may result in a dilutional acidosis and an increasing base deficit, it may cloud clinical decision making when resuscitative efforts are guided by acid-base status on routine arterial blood gas analysis. This is a prospective, randomized study to evaluate changes in acid-base and electrolyte (sodium, potassium, calcium) status with the use of various isotonic fluids for intraoperative resuscitation.

Conditions Studied

Interventions

  • DRUG Normal Saline
  • DRUG Lactated Ringer
  • DRUG Normosol-R Inj

Study Locations (1)

Ohio

  • Nationwide Children's Hospital - Columbus

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2017-02-23
Est. Completion 2018-09-30
Phase Phase 3

Sponsor

Nationwide Children's Hospital

188 total trials

What the Registry Record Tells You About NCT03054922

The ClinicalTrials.gov registry entry for NCT03054922 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 59 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 109,409-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The listed sponsor is Nationwide Children's Hospital, which has 188 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Anesthesia appearing as the primary indexed condition, and to 3 interventions - of which Normal Saline is the first listed.

NCT03054922 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT03054922 about?

NCT03054922 is a clinical study titled "Impact of Intraoperative Fluid Management on Electrolyte and Acid-base Variables". During major surgical procedures, intravascular volume is maintained with the administration of isotonic fluids such as Lactated Ringers (LR), Normal Saline (NS) or Normosol-R. All three of these fluids are in common clinical use for this purpose. As large volumes of NS may result in a dilutional ac...

What is the current status of trial NCT03054922?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 59 participants. The study started on 2017-02-23. Estimated completion is 2018-09-30.

What conditions does trial NCT03054922 study?

This clinical trial studies the following conditions: Anesthesia.

What interventions are being tested in trial NCT03054922?

The interventions under investigation include: Normal Saline (DRUG), Lactated Ringer (DRUG), Normosol-R Inj (DRUG).

Who is sponsoring clinical trial NCT03054922?

This trial is sponsored by Nationwide Children's Hospital, which has 188 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03054922 being conducted?

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

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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.