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Overnight and In-house 3D-printed Patient-specific Casts for Non-operative Treatment of Distal Radius Fractures

NCT05346926 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2022-04-26

No results posted yet for this study

Summary

The aim of this prospective randomized trial is the acquisition and evaluation of data to assess the relevance, feasibility and safety of forearm casts based on 3D-printing technology in the nonoperative treatment of distal radius fractures.

Conditions

  • Radius Fracture Distal

Interventions

DEVICE

3D-printed cast

The 3D-printed casts are produced using 3D print technology based on software by Belgian software company: The patient's forearm is scanned with a tablet (duration: approx. 5 min), whereupon the cast is printed overnight according to the scan (duration: approx. 4h) and adjusted to the patient during the next appointment.

DEVICE

Conventional cast

A conventional plaster cast is applied for treatment of the distal radius fracture.

Sponsors & Collaborators

  • Spentys

    collaborator INDUSTRY

  • Alissa Gubeli

    lead OTHER

Principal Investigators

  • Philipp Honigmann, PD Dr. med. · Cantonal Hosptal, Baselland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-01
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • Switzerland

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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 NCT05346926 on ClinicalTrials.gov