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Effects of Using the Duracore Splinting Device on Patient Outcomes Related to Chest Trauma

NCT04909463 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2025-05-14

Study results available
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Summary

The purpose of this study is to use the Duracore splinting device to measure lung capacities of patients with rib fractures in control and experimental groups to determine if lung capacities improve with the splint.

Conditions

  • Rib Fractures
  • Rib Fracture Multiple

Interventions

DEVICE

Chest Splint

Those receiving intervention will be given the Duracore chest splint for use throughout the trial.

Sponsors & Collaborators

  • CommonSpirit Health

    lead OTHER

Principal Investigators

  • Trenton Bradbury, BS · CommonSpirit Health

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-12-04
Primary Completion
2021-07-30
Completion
2021-07-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04909463 on ClinicalTrials.gov