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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00610220
Other study ID # 1000010377
Secondary ID
Status Completed
Phase Phase 4
First received January 24, 2008
Last updated October 6, 2017
Start date January 2007
Est. completion date October 2009

Study information

Verified date May 2014
Source The Hospital for Sick Children
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will compare the effectiveness of a prefabricated wrist splint with thermoplast reinforcements versus a short arm cast in skeletally immature children.

The hypothesis is that the commercially available wrist splint is at least as effective as traditional casting with respect to recovery of physical function.


Description:

Acceptability angulated wrist bone fractures in children carry an excellent long-term prognosis because of the unique capacity of skeletally immature bones to heal via remodeling. Their management varies widely and there is virtually no scientific evidence supporting one treatment modality over another. Importantly, the most common treatment modality of cast application for four to six weeks is associated with many inconveniences. There are commercially available wrist splints that offer a more convenient alternative. Wrist splints likely have comparable immobilization and symptom relief, while simultaneously allowing for easier bathing and less reliance on subspeciality care. Preliminary adult evidence suggests that, in a comparable adult fracture, splinting may offer a safe alternative to casting, with earlier resumption of the usual activities. However, this treatment modality needs to be compared to the traditional casting management in the pediatric population before it can be recommended for clinical practice.

This study will be the first to challenge the current practice of routine casting and compare it to a commercially available wrist splint with respect to recovery of physical function in children with acceptably angulated wrist fractures. In addition, standardized treatment of these fractures with a splint may be associated with lower morbidity, reduced use of health care resources, and have the potential for cost savings.

This study will compare, in skeletally immature children, the functional outcomes that result from treatment with a prefabricated wrist splint versus a short arm cast in acceptably angulated distal radius fractures. Secondly, the cost-effectiveness of the splint relative to the cast will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date October 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender All
Age group 5 Years to 12 Years
Eligibility Inclusion Criteria:

1. Skeletally immature children.

2. Children must have a bone age of = 5 years of age.

3. Less than or equal to 15° angulation in the sagittal plane and = 0.5 cm displacement in the frontal plane.

Therefore, all skeletally immature children = 5 years and with a bone age of = 11 years who present to the ED of HSC with acute distal metaphyseal radius +/- ulnar fractures that meet criteria for acceptable angulation and displacement will be eligible for enrollment.

Exclusion Criteria:

1. Age < 5 years or > 12

2. The following diagnoses of distal radius fracture: buckle fracture, growth plate fractures of any kind, distal radius metaphyseal fractures with greater than 15° of angulation in the sagittal plane and/or more than 0.5 cm of displacement in the frontal plane.

3. All open fractures which require a surgical debridement.

4. All children at risk for pathological fractures such as those with congenital or acquired generalized bony disease. Stricter immobilization and a different prognosis may be applicable to this population.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Fiberglass short arm cast
Cast will be applied for a 4-week period
Prefabricated wrist splint
Splint will be applied for a 4-week period

Locations

Country Name City State
Canada The Hospital for Sick Children Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
The Hospital for Sick Children

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Boutis K, Willan A, Babyn P, Goeree R, Howard A. Cast versus splint in children with minimally angulated fractures of the distal radius: a randomized controlled trial. CMAJ. 2010 Oct 5;182(14):1507-12. doi: 10.1503/cmaj.100119. Epub 2010 Sep 7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Modified performance Activities Scale for Kids (ASKp) score 6 weeks
Secondary Changes in Angulation and/or displacement 1 and 4 weeks
Secondary Pain 1 and 4 weeks
Secondary Duration of immobilization device 1 and 4 week follow-up visits
Secondary Grip Strength 6 week follow-up visit
Secondary Range of Motion Week 6
Secondary Patient Preference for their Device Week 6
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