Characteristics and Safety Profiles of Hydrocolloid Polyester Dressing

Phase 1

Completed

• Conditions: Trauma Wound; wound dressing, pain, wound adherent, skin irritation

• Registration Number: TCTR20211007002
• Lead Sponsor: Siriraj hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2021-04-01
• Study Start: 2021-10-07
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 72

Inclusion Criteria

patients who aged between 18 to 80 years old, with more than 10 cm2 in area, and had injured wound on arms or legs were recruited in this study.

Exclusion Criteria

volunteer who had a history of allergic to dressing, Herbs (Aloe vera, Centella asiatica), signs of wound infection, a previous history of chronic pain or psychotic disease.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain asssessment 24 hours Numeric Rating Scale

Secondary Outcome Measures

Name	Time	Method
Dressing removal evaluation 24 hours dressing removal evaluation