ClinicalTrials.Veeva

Menu

Study on Wood-plastic Composite for Circumferential Casting (WOODCAST)

O

Onbone

Status

Completed

Conditions

Ankle Fracture
Radius Fracture
Bone Fracture

Treatments

Other: limb casting/splinting

Study type

Interventional

Funder types

Industry

Identifiers

NCT01493167
37/13/03/02/2011

Details and patient eligibility

About

The purpose of study is to verify that WOODCAST Circular system performs safely and effectively in its intended use.

Full description

An ecologically friendly and biodegradable wood-plastic composite-cast is studied. The purpose of the study is to verify that WOODCAST Circular system performs safely and effectively in its intended use. Patients, who need immobilization of extremity (including for example scaphoid fracture of the wrist or ankle fracture) will be participating in the study. Various casting techniques with novel WOODCAST material will be studied.

Enrollment

97 patients

Sex

All

Ages

Under 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patient treatment involves circular casting;
  • age 0-90 years;
  • mother tongue finnish or swedish

Exclusion criteria

  • open fracture;
  • other fractures or a previous fracture;
  • a previous or simultaneous tendon-, nerve-, or vascular injury to the extremity yo be treated;
  • a multiple injured extremity;
  • decreased co-operation of the patient;
  • malignancy;
  • an illness affecting the general health.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

97 participants in 1 patient group

limb casting/splinting
Other group
Description:
Patient age 0-90 years. Patient treatment requires extremity immobilization
Treatment:
Other: limb casting/splinting

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems