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Efficacy of Baby Talcum in Prevention of Pruritus Assosiated With Cast

NCT01017315 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2012-05-15

No results posted yet for this study

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.

Conditions

  • Fracture Distal Radius

Interventions

DRUG

Baby talcum

50 grams apply locally prior cast application

Sponsors & Collaborators

  • Prince of Songkla University

    lead OTHER

Principal Investigators

  • Boonsin Tangtrakulwanich, MD.,Ph.D · Prince of Songkla University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
15 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2012-07-31
Completion
2012-10-31

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01017315 on ClinicalTrials.gov