CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 200 enrolled
Drug / intervention
Audiovisual distraction device +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04238572
NCT04238572N/ACompleted
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Evaluation of an Immersive Audiovisual Distraction Device Impact on Peroperative Opioid Consumption. A Prospective Randomized Controlled Study

University Hospital, Caen·interventional·Posted Jan 23, 2020·Updated Aug 3, 2021

In Brief

A clinical study evaluating Audiovisual distraction device and Analgesia nociception index for Surgical Procedure, Unspecified and 2 related conditions. Completed, enrolled 200 participants across 1 site.

Detailed Summary

This study evaluate the impact of an audiovisual distraction device on the peroperative opioid consumption for outpatient procedures with Remifentanil added to local anesthesia. Half of patients will receive an audiovisual distraction device while the other half not.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgical Procedure, Unspecified, Analgesia, Outpatient
CountriesFrance
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedJan 23, 2020
Enrollment StartFeb 19, 2020
Primary CompletionJan 1, 2021
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 6.4 years ago

Interventions

Audiovisual distraction devicedevice

Evaluate the impact of an audiovisual distraction device on the peroperative opioid consumption

Analgesia nociception indexdevice

ANI (Analgesia Nociception Index) will be used for peroperative overall comfort measurement