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COMPLETED NA

The Effect of Higher Protein Dosing in Critically Ill Patients

NCT03160547 · View on ClinicalTrials.gov ↗

Study Summary

The investigator will investigate the effects of higher protein/amino acid dosing (≥2.2 g/kg/d) vs usual protein/amino acid dosing (≤1.2 g/kg/d) on clinical outcomes in nutritionally high risk ill patients.

Interventions

  • OTHER Usual Protein/Amino Acid Group
  • OTHER Higher Protein/Amino Acid Group

Study Locations (20)

New Jersey

  • Virtua — Marlton
  • Virtua — Mount Holly
  • Virtua — Voorhees Township

Arizona

  • Banner University Medical Center — Phoenix
  • Phoenix VA Health Care System — Phoenix

Illinois

  • NorthShore University HealthSystem — Evanston
  • SwedishAmercian.Hospital — Rockford

Ohio

  • The Ohio State University Wexner Medical Center — Columbus
  • Fairfield Medical Center — Lancaster

Tennessee

  • University of Tennessee Medical Center Knoxville — Knoxville
  • Vanderbilt University Medical Center — Nashville

Washington

  • Harborview Medical Center — Seattle
  • Legacy Salmon Creek Medical Center — Vancouver

California

  • MemorialCare Long Beach Medical Center — Long Beach

Indiana

  • IU Health Methodist Hospital — Indianapolis

Trial Details

FieldValue
Enrollment Target 1,329 participants
Start Date 2017-11-21
Est. Completion 2021-12-03
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03160547

The ClinicalTrials.gov registry entry for NCT03160547 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,329 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clinical Evaluation Research Unit at Kingston General Hospital, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Critical Illness appearing as the primary indexed condition, and to 2 interventions — of which Usual Protein/Amino Acid Group is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03160547 reports 20 study locations spanning 13 distinct geographic areas — top geographies include New Jersey, Arizona, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03160547 about?

NCT03160547 is a clinical study titled "The Effect of Higher Protein Dosing in Critically Ill Patients". The investigator will investigate the effects of higher protein/amino acid dosing (≥2.2 g/kg/d) vs usual protein/amino acid dosing (≤1.2 g/kg/d) on clinical outcomes in nutritionally high risk ill patients.

What is the current status of trial NCT03160547?

This trial is currently completed. It is a NA study. The enrollment target is 1,329 participants. The study started on 2017-11-21. Estimated completion is 2021-12-03.

What conditions does trial NCT03160547 study?

This clinical trial studies the following conditions: Critical Illness, Malnutrition. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03160547?

The interventions under investigation include: Usual Protein/Amino Acid Group (OTHER), Higher Protein/Amino Acid Group (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03160547?

This trial is sponsored by Clinical Evaluation Research Unit at Kingston General Hospital, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03160547 being conducted?

This trial has 20 study locations across Arizona, California, Illinois, Indiana, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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