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Evaluation of Splinting in Tetraplegia

NCT04523636 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2020-08-21

No results posted yet for this study

Summary

This study compared pre-fabricated and custom resting hand splints among people who were in inpatient rehabilitation after a cervical spinal cord injury.

Conditions

  • Spinal Cord Injury Cervical
  • Splints

Interventions

DEVICE

Splinting

Pre-fabricated or custom resting hand splints

Sponsors & Collaborators

  • University of Maryland, Baltimore

    collaborator OTHER

  • The Craig H. Neilsen Foundation

    collaborator OTHER

  • Thomas Jefferson University

    lead OTHER

Principal Investigators

  • Peter Gorman, MD · University of Maryland, Baltimore

  • Paula Geigle, PhD · University of Maryland, Baltimore

  • Sara Frye, MS · Thomas Jefferson University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-04
Primary Completion
2018-12-20
Completion
2018-12-20

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 NCT04523636 on ClinicalTrials.gov