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Clinical Trials/NCT05346926
NCT05346926
Completed
Not Applicable

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

Alissa Gubeli1 site in 1 country40 target enrollmentMarch 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Radius Fracture Distal
Sponsor
Alissa Gubeli
Enrollment
40
Locations
1
Primary Endpoint
Score of clinical effectiveness questionnaire
Status
Completed
Last Updated
4 years ago

Overview

Brief 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.

Detailed Description

The study design is planned according to similar studies investigating the treatment of distal radius fractures. Upon the patient's arrival at the emergency unit, the distal radius fracture is examined following the same scheme as before. The wrist is x-rayed in two planes. If there is a distal radius fracture and none of the exclusion criteria apply, the patient is included in the study after giving their consent in writing. The patients are then assigned to the "conventional cast" group (Group A) or the "3D print cast" group (Group B) in randomized trial, either immediately during the emergency consultation or within a week during hand surgery consultation hours. For initial immobilization, a thermoplastic cast splint is used as before. Depending on the randomization, the cast is changed to a Scotchcast cast (Group A) or a 3D printed cast (Group B). Further treatment of both groups occurs based on the same algorithm as before (see below). The cast for Group B are produced using 3D print technology based on software by a Belgian company, our collaborators: 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. The patients are examined after 1, 6, 12, 26 and 52 weeks in the outpatient clinic. Follow up x rays, patient satisfaction and clinical efficacy questionnaires and clinical examinations are conducted.

Registry
clinicaltrials.gov
Start Date
March 1, 2020
End Date
December 31, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Alissa Gubeli
Responsible Party
Sponsor Investigator
Principal Investigator

Alissa Gubeli

Junior Consultant Hand Surgery

Kantonsspital Baselland Bruderholz

Eligibility Criteria

Inclusion Criteria

  • Informed Consent as documented by signature (Appendix Informed Consent Form)
  • Undisplaced or minimally displace distal radius fractures

Exclusion Criteria

  • Age \< 18yrs.
  • Dorsal dislocation (dp angle) \>20°
  • Palmar dislocation
  • Ad latus dislocation
  • Radio-/ulnar angulation in the coronary plane
  • Symptoms of neurologic affection (Median nerve)
  • Bilateral fractures
  • Previous ipsilateral distal radius fracture
  • The patient is unable to give informed consent due to physical or mental impairment
  • The patient is unavailable for follow-up examinations (foreign country, Polytrauma, etc)

Outcomes

Primary Outcomes

Score of clinical effectiveness questionnaire

Time Frame: 1 year

quantified with questionnaire (0-12, 0=worst result)

Score of modified patient satisfaction questionnaire

Time Frame: 1 year

quantified with questionnaire (0-12, 0=worst result)

Secondary Outcomes

  • Fracture healing(1 year)
  • Amount of grip strength in (N/kg)(1 year)
  • Score of Disabilities of Arm, Shoulder and Hand(1 year)
  • Score on Visual Analogue Pain Scale(1 year)
  • Amount of range of motion in degrees(1 year)

Study Sites (1)

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