Comparison Study on Hair Apposition Technique Performed Between Nurses and Doctors in Emergency Department.

February 9, 2017 updated by: Singapore General Hospital

A Single-blinded Comparative Study on Hair Apposition Technique Performed Between Nurses and Doctors in Emergency Department.(HAT2 Study)

The purpose of this study is to compare the effectiveness, complications and benefits of Hair Apposition Technique(HAT)performed by nurses or doctors.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Hair Apposition Technique (HAT) is a relatively new technique for treating certain scalp lacerations. It has been shown to be equally acceptable as compared to the standard toilet and suture. This procedure has been the technique of choice for suitable scalp lacerations in Department of Emergency Medicine, Singapore General Hospital (DEM, SGH) and Emergency Medicine Department, National University Hospital (EMD, NUH).

Currently HAT is being performed by doctors in the respective hospitals. Nurses, on the other hand, are routinely using tissue adhesives for minor wound closure. However, nurses in Kandang Kerbau Women and Children Hospital (KKWCH) have been routinely using HAT for 1 year now. Studies had been also been done by nurses in treating of minor wounds using various tissue adhesives as well as hair knotting technique.The trend of nurses handling minor wounds with tissue adhesives, hair knotting technique as well as HAT suggested the possibility of nurses performing HAT to a degree as competent as a doctor.

This study aims to compare the effectiveness, complications and benefits HAT performed between nurses and doctors in the Emergency Department.

Study Type

Interventional

Enrollment

360

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Singapore
      • Singapore, Singapore, 169608
        • Singapore General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • All age group
  • Linear lacerations of scalp
  • Lacerations less than 10cm in length
  • Hair at least 3cm in length

Exclusion Criteria:

  • Severely contaminated wounds
  • Actively bleeding wounds
  • Patients with unstable vital signs or altered mental state

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Single

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Presence of any complications, namely infection, scarring, bleeding, wound breakdown and allergy
Satisfactory wound healing

Secondary Outcome Measures

Outcome Measure
Pain perception
Duration of procedure

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Singapore General Hospital

Investigators

  • Principal Investigator: Ong EH Marcus, M.D, Singapore General Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2002

Study Completion

February 1, 2005

Study Registration Dates

First Submitted

July 17, 2006

First Submitted That Met QC Criteria

July 17, 2006

First Posted (Estimate)

July 19, 2006

Study Record Updates

Last Update Posted (Actual)

February 10, 2017

Last Update Submitted That Met QC Criteria

February 9, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DCR/P15/2003

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Scalp Laceration

Clinical Trials on Hair Apposition Technique

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Netherlands

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe