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Clinical Trial Summary

This study aims to evaluate the efficacy of baby talcum in prevent pruritus after cast application in orthopaedic patients.

The investigators will do a randomized controlled trial in patient with fracture distal end of radius treated conservatively.

Pruritus score and satisfaction will be monitor along the entire course of cast retention.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01017315
Study type Interventional
Source Prince of Songkla University
Contact
Status Enrolling by invitation
Phase Phase 3
Start date July 2009
Completion date October 2012

See also
  Status Clinical Trial Phase
Completed NCT05521464 - Robert Jones Bandage Versus Cast in the Treatment of Distal Radius Fracture in Children N/A
Recruiting NCT05131685 - Distal Radius Interventions for Fracture Treatment N/A