Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01992120 · ClinicalTrials.gov registry record · NA

Utility of High-Fidelity Simulation In the Education and Assessment of Residents in the Recognition and Management of the Sepsis Syndrome

A NA study, sponsored by NYU Langone Health.

Terminated
Registry status
NA
Development phase
40
Enrollment target

NCT01992120: Clinical Trial NA study, sponsored by NYU Langone Health.

NCT01992120 is a NA study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01992120, a NA study, was terminated before completion, sponsored by NYU Langone Health.

TERMINATED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The primary objective of the proposed study will be to determine if a multi-modality teaching curriculum utilizing high-fidelity simulation and didactic lecture will result in sustained improvement by internal medicine residents in written knowledge and clinical performance when compared to residents receiving a curriculum utilizing only didactic lecture. The investigators hypothesis is that the addition of high-fidelity simulation to a traditional didactic lecture curriculum will result in sustained and superior written knowledge and practical performance when compared to a group receiving only didactic lecture on the same topic. Specifically, the investigators will be assessing internal medicine resident knowledge and performance in the area of sepsis in the hospitalized patient, and will shape the investigators teaching curriculum around this focus.

Primary Outcome

Written test

Interventions

  • OTHER Debriefing of high-fidelity sepsis simulation scenarios
  • OTHER Placebo: Debriefing of high-fidelity non-sepsis simulation scenarios

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2013-11
Est. Completion 2014-07
Phase NA
NYU Langone Health

1,164 total trials

Why NCT01992120 stopped before completion

NCT01992120 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Debriefing of high-fidelity sepsis simulation scenarios is the first listed.

NCT01992120 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01992120 about?

NCT01992120 is a clinical study titled "Utility of High-Fidelity Simulation In the Education and Assessment of Residents in the Recognition and Management of the Sepsis Syndrome". The primary objective of the proposed study will be to determine if a multi-modality teaching curriculum utilizing high-fidelity simulation and didactic lecture will result in sustained improvement by internal medicine residents in written knowledge and clinical performance when compared to resident...

What is the current status of trial NCT01992120?

This trial is currently terminated. It is a NA study. The enrollment target is 40 participants. The study started on 2013-11. Estimated completion is 2014-07.

What interventions are being tested in trial NCT01992120?

The interventions under investigation include: Debriefing of high-fidelity sepsis simulation scenarios (OTHER), Placebo: Debriefing of high-fidelity non-sepsis simulation scenarios (OTHER).

Who is sponsoring clinical trial NCT01992120?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01992120's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01992120, the US trial registry maintained by the National Library of Medicine. NCT01992120 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.