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Clinical Application and Validation of Innovative Tourniquet

Not Applicable
Completed
Conditions
Compartment Syndrome of Forearm
Interventions
Device: Innovative tourniquet (Acusense Nonpneumatic tourniquet)
Registration Number
NCT05605990
Lead Sponsor
National Cheng-Kung University Hospital
Brief Summary

Background: Tourniquets are the basic equipment for nurses to perform blood draws, and venous indwelling needles for congestion, or for hemostasis. Therefore, forgetting to remove the tourniquet is a common problem that leads to blood circulation being blocked, and even severe tissue necrosis occurred.

Purpose: The study aimed to evaluate whether this innovative tourniquet could prevent forgetting to remove the tourniquet, and improve the satisfaction of care.

Research design: This clinical research trial was a quasi-experimental study designed for a single group with pre-and post-test. We will recruit 160 nurses in high-risk units of the hospital. The delay in removing the tourniquet as our study outcome is defined as the removing time delay of one minute.

Expected results: The research results will provide some evidence of the efficacy of intelligent tourniquets.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
160
Inclusion Criteria

Nurse group: We included nurses who have working experience of more than 3 months, and are willing to use an innovative tourniquet.

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Nurse groupInnovative tourniquet (Acusense Nonpneumatic tourniquet)Using an innovative tourniquet (Acusense Nonpneumatic tourniquet) for the standard of care
Primary Outcome Measures
NameTimeMethod
Preventing the forgetting to remove the tourniquetA three months period

Forgetting to remove the tourniquet is defined as the optimal removing time to delay of one minute.

Enhancing nurses' satisfactionA three months period

The Likert Scale asks how much a person agrees or disagrees with a particular statement or question. It is usually made up of a 5-point rating scale ranging from 1 and 5 with 10-item.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan

🇨🇳

Tainan, Taiwan

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