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

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University (Other)
Overall Status
Completed
CT.gov ID
NCT04938674
Collaborator
(none)
177
1
11
16.1

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Device: ultrasonic guidance

Detailed 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.

Study Design

Study Type:
Observational
Actual Enrollment :
177 participants
Observational Model:
Case-Crossover
Time Perspective:
Cross-Sectional
Official Title:
Application of Ultrasonic Guided Puncture in Blood Collection in Patients With Severe Trauma
Actual Study Start Date :
Apr 1, 2020
Actual Primary Completion Date :
Mar 1, 2021
Actual Study Completion Date :
Mar 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Standard process for blood collection using Ultrasonic Guided puncture

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

Outcome Measures

Primary Outcome Measures

  1. Satisfaction analysis of the patient's family members [1 year]

    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.

  2. Time index of nursing treatment for patients with severe trauma [1 year]

    In contrast to the control group,time required for blood collection in patients with severe trauma

  3. Satisfaction analysis of the doctors [1 year]

    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

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ① airway obstruction, need tracheal intubation or intubation;② breathing stop, respiratory distress or significant slowing down;③ circulatory system shows various shock signs④GCS≤8;⑤ 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China Zhejiang Zhejiang China 310000

Sponsors and Collaborators

  • Second Affiliated Hospital, School of Medicine, Zhejiang University

Investigators

  • Principal Investigator: Chen Ze Xin, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Second Affiliated Hospital, School of Medicine, Zhejiang University
ClinicalTrials.gov Identifier:
NCT04938674
Other Study ID Numbers:
  • 2021-0272
First Posted:
Jun 24, 2021
Last Update Posted:
Jun 24, 2021
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Second Affiliated Hospital, School of Medicine, Zhejiang University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 24, 2021