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Evaluation of the Efficacy of VR on Pain and Anxiety When Performing an Ultrasound-controlled Ankle Block.

NCT03677323 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2019-03-26

No results posted yet for this study

Summary

The purpose of this study is to observe or not a reduction on pain and anxiety felt by the patient when performing an ultrasound-controlled ankle block in preparation for forefoot surgery, using a virtual reality device instead of drug sedation.

Conditions

  • Hallux Valgus
  • Surgery

Interventions

DEVICE

Virtual reality

The patient will have the choice between different environments and the use of this device will remain under the control of the medical team. The patient will wear the virtual reality device at the time of the completion of the ankle block and will remove it once the nerve puncture is complete.

DRUG

Droleptan

Venous administration of 1.25 mg of Droleptan

DRUG

Propofol

Venous administration of 20 mg of Propofol

DRUG

Sufentanyl

Venous administration of 5 μg of Sufentanyl.

Sponsors & Collaborators

  • Clinique Saint Jean, France

    lead OTHER

Principal Investigators

  • Thomas PILLANT, MD · Clinique Saint Jean, Montpellier

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-02
Primary Completion
2019-02-21
Completion
2019-02-21

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03677323 on ClinicalTrials.gov