NCT07350525

CASTomize 4D Printed Cast Versus Fibreglass Casts for Distal Radius Fractures

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 25 (actual)
• Sponsor: Tan Tock Seng Hospital · Academic / Other
• Sex: All
• Age: 21 Years
• Healthy volunteers: Not accepted

Summary

This study is a randomised control trial comparing Castomize 4D printed cast versus conventional fibreglass casts in isolated conservatively treated distal radius fractures. The primary outcome measure is fracture reduction. Secondary outcome measures include patient reported outcome measures such as the Adult Rated Cast Evaluation Questionnaire (ARCEQ), comfort of the cast, quality of life assessed with the EQ-5D-5L questionnaire, cost-effectiveness and adverse events occurrence. In total, 30 patients will be included and followed for 6 months.

Conditions

• Distal Radius Fracture

Interventions

Type	Name	Description
DEVICE	Castomize cast	4D castomize cast for distal radius fracture immobilisation
OTHER	Control	Standard of care casting

Timeline

• Start date: 2024-01-14
• Primary completion: 2025-06-01
• Completion: 2025-12-25
• First posted: 2026-01-20
• Last updated: 2026-01-20

Locations

1 site across 1 country: Singapore