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

NCT03162354 · ClinicalTrials.gov registry record · NA

The CDR Implementation Trial

A NA study, sponsored by Milton S. Hershey Medical Center.

Completed
Registry status
NA
Development phase
420
Enrollment target

NCT03162354: Completed NA study, sponsored by Milton S. Hershey Medical Center.

NCT03162354 is a NA study that has completed, run by Milton S. Hershey Medical Center. The registered enrollment target is 420 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03162354, a NA study, has completed, sponsored by Milton S. Hershey Medical Center.

COMPLETED
Registry status
NA
Development phase
420 participants
Enrollment target

Study Summary

To increase the accuracy of doctors' decisions to launch or forgo child abuse evaluations in their young, acutely head-injured patients, investigators have derived and validated a clinical decision rule (CDR) that detects abusive head trauma (AHT) with 96% sensitivity in pediatric intensive care unit (PICU) settings. This "CDR Implementation Trial" across eight PICU sites will assess the CDR's actual impact on AHT screening accuracy, identify factors associated with maximal physician acceptance and application of this novel AHT screening tool, and assess the sustainability of active CDR implementation strategies.

Primary Outcome

This outcome measure facilitates a comparison of the percentage of patients that the clinical decision rule stratified as higher risk who were evaluated thoroughly for abuse (with both skeletal survey and retinal exam) at intervention vs. control sites. We hypothesized that thorough evaluations of higher risk patients would be significantly higher at intervention sites.

Interventions

  • OTHER Application of a validated Clinical Decision Rule (CDR) as an AHT screening tool

Trial Details

FieldValue
Enrollment Target 420 participants
Start Date 2017-08-01
Est. Completion 2020-03-31
Phase NA
Milton S. Hershey Medical Center

396 total trials

What the finished NCT03162354 record still lists

NCT03162354 is an interventional study that assigns participants to a tested intervention. The registered 420 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 1 intervention - of which Application of a validated Clinical Decision Rule (CDR) as an AHT screening tool is the first listed.

NCT03162354 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03162354 about?

NCT03162354 is a clinical study titled "The CDR Implementation Trial". To increase the accuracy of doctors' decisions to launch or forgo child abuse evaluations in their young, acutely head-injured patients, investigators have derived and validated a clinical decision rule (CDR) that detects abusive head trauma (AHT) with 96% sensitivity in pediatric intensive care uni...

What is the current status of trial NCT03162354?

This trial is currently completed. It is a NA study. The enrollment target is 420 participants. The study started on 2017-08-01. Estimated completion is 2020-03-31.

What interventions are being tested in trial NCT03162354?

The interventions under investigation include: Application of a validated Clinical Decision Rule (CDR) as an AHT screening tool (OTHER).

Who is sponsoring clinical trial NCT03162354?

This trial is sponsored by Milton S. Hershey Medical Center, which has 396 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03162354's enrollment target sits among peer trials

420 239th of 2000 higher than 1,761 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

  • NCT01790152 · 420 participants

    Effects of Dexrazoxane Hydrochloride on Biomarkers Associated With Cardiomyopathy and Heart Failure After Cancer Treatment

  • NCT02701244 · 420 participants

    A Registry Study of Breast Microseed Treatment

  • NCT02966665 · 420 participants · Phase 1

    : Vascular Function in Health and Disease

  • NCT04149743 · 420 participants · NA

    HEMOTAG® Assessment for Short-term Outcomes of Heart Failure

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03162354, the US trial registry maintained by the National Library of Medicine. NCT03162354 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.