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

NCT04388423 | Unknown DMC

• 1 other identifier: PLAGHAOC202003
• Study Type: interventional
• Target: 240
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Transversus Abdominis Plane Block; Simulation Training; Learning Curve

Outcome Measures

Primary Outcomes (1)

• 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

Study Arms (2)

Group S

EXPERIMENTAL

Other: simulated puncture training

Group C

EXPERIMENTAL

Other: traditional bedside teaching

Interventions

simulated puncture training OTHER

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.

Group S

traditional bedside teaching OTHER

The residents are trained by traditional bedside teaching

Group C

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

• 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.

Sponsors & Collaborators

• Chinese PLA General Hospital: lead

Study Sites (1)

Chinese PLA General Hospital

Beijing, Haidian, 100853, China

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: May 12, 2020
• First Posted: May 14, 2020
• Study Start: May 15, 2020
• Primary Completion: December 31, 2020
• Study Completion: January 1, 2021
• Last Updated: July 14, 2020

Record last verified: 2020-07

Locations

CN (1)