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NCT04388423 Clinical Trial

Study on Application of Simulated Training in Ultrasound Guided Transversus Abdominis Plane Block

Simulation Training Clinical Trial

Official title:
Study on Application of Simulated Training in Ultrasound Guided Transversus Abdominis Plane Block

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT04388423
Other study ID # PLAGHAOC202003
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date May 15, 2020
Est. completion date January 1, 2021

Study information
Verified date July 2020
Source Chinese PLA General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

With the development of society and the enhancement of people's awareness of law and self-protection, it is necessary to use simulation technology to create a simulated human and clinical environment to replace the traditional teaching of clinical operation on real patients. So simulation teaching is more and more important in medical education. However, simulation teaching is in the ascendant in China, especially in the ultrasound-guided nerve block, limited by the lack of full simulation of puncture model, the simulation training of ultrasound-guided nerve block is not carried out much. Therefore, this study uses simulation training to carry out ultrasound-guided horizontal abdominal muscle block teaching, in order to explore an effective way of ultrasound-guided nerve block teaching.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 240
Est. completion date January 1, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- 18-70 years old; ASA 1 ~ 2; patients under non-transvaginal gynecologic surgery, rectal surgery or descending colon surgery

Exclusion Criteria:

- Patients with communication disorder Central or peripheral nervous system diseases. Liver and kidney functions seriously damaged Coagulation function abnormality and local anesthetic allergy history Patients with serious heart disease, hypertension and diabetes. Patients who have used analgesic drugs or drugs that may affect cardiovascular function within 24 hours before operation.

Patients with infection at the puncture site.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• simulated puncture training
The residents are trained of simulated puncture : 1.the location puncture; 2. finding fixed-point needle on the model for 5 times, each time for 30 minutes.
• traditional bedside teaching
The residents are trained by traditional bedside teaching

Locations
Country Name City State
China Chinese PLA General Hospital Beijing Haidian

Sponsors (1)
Lead Sponsor Collaborator
Chinese PLA General Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary The time taken to complete the blocking operation After finishing the disinfection sheet, the operator began to perform unilateral transversal muscle planar ultrasound scanning, positioning and puncture until the end of injection. procedure/surgery
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