Author-Wang Ping-- Research：Application of Ultrasonic Guided Puncture in Blood Collection in Patients With Severe Trauma

Severe Trauma Clinical Trial

Official title:

Application of Ultrasonic Guided Puncture in Blood Collection in Patients With Severe Trauma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04938674
• Other study ID #: 2021-0272
• Status: Completed
• Start date: April 1, 2020
• Est. completion date: March 1, 2021

Study information

• Verified date: April 2020
• Source: Second Affiliated Hospital, School of Medicine, Zhejiang University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study aimed to investigate the application of ultrasound guided puncture technique in blood collection in patients with severe trauma. The methods of this study is 93 patients with severe trauma were selected from the emergency room of the Second Affiliated Hospital of Zhejiang University from April 2020 to September 2,2020 and from October 2020 to March 2021, comparing the differences between nursing treatment efficiency and doctor satisfaction.

Description:

Standard process for blood collection using Ultrasonic Guided puncture.The control group used the traditional blood sample collection process, which was mainly based on personal clinical experience. Statistical analysis using SPSS 25.0 statistical software. Observation index are time index of nursing treatment for patients with severe trauma: the time required for acquisition time, disposable puncture success rate, blood routine and blood type delivery time, rescue room stay time, etc and patient family and doctor satisfaction analysis: self-designed questionnaire, family satisfaction process, service time, service attitude, rescue technology, health education, including advice time, nursing quality, medical communication, teamwork, service attitude, evaluation levels: very satisfaction, satisfaction and dissatisfaction.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 177
• Est. completion date: March 1, 2021
• Est. primary completion date: March 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• ? airway obstruction, need tracheal intubation or intubation;? breathing stop, respiratory distress or significant slowing down;? circulatory system shows various shock signs?GCS=8;? body table visible head, torso, chest open injury or yoke chest

Exclusion Criteria:

• All patients who stop the rescue room trauma evaluation and treatment midway through hospital transfer and automatic discharge

Related Conditions & MeSH terms

• Severe Trauma
• Wounds and Injuries

Intervention

Device:
• ultrasonic guidance
Standard process for blood collection using Ultrasonic Guided puncture

Locations

Country	Name	City	State
China	2nd Affiliated Hospital, School of Medicine, Zhejiang University, China	Zhejiang	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Satisfaction analysis of the patient's family members	In contrast to the control group,patient family satisfaction survey includes medical time. The evaluation level is divided into 3 categories: very satisfied, satisfactory and unsatisfactory.	1 year
Primary	Time index of nursing treatment for patients with severe trauma	In contrast to the control group,time required for blood collection in patients with severe trauma	1 year
Primary	Satisfaction analysis of the doctors	In contrast to the control group,physician satisfaction survey includes executive advice time.The evaluation level is divided into 3 categories: very satisfied, satisfactory and unsatisfactory	1 year