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Clinical Trials in France / NCT06928740
Recruiting Not applicable

Efficacy on Anxiety of the Digital Music Application Versus Equimolar Mixture of Oxygen and Nitrous Oxide in Patients Receiving CT-guided Lumbar Infiltration

NCT06928740 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-10-21
Last updated
2026-02-20

Condition(s) studied

Low Back PainAnxiety

Investigational drug(s) / intervention(s)

Music Care® deviceEMONO

Music Care® device: Installation of the Music Care® device, selection of the sequence based on the patient's musical taste, listening to at least 20-minute sequence in the preparation room. Once placed on the scanner table, the patient listens to the same sequence as in the preparation room.

EMONO: Equimolar mixture of oxygen and nitrous oxide given as usual care

Study summary

Since the Covid-19 crisis, patients appear more stressed, with increasing fear of exams and the hospital environment, in particular for CT scan teams, which require injections. Currently, an equimolar mixture of oxygen and nitrous oxide (EMONO) is used to calm patients. However, the patient's prone position complicates its use, with patients sometimes in painful position and the discomfort of gas inhalation (nausea, dizziness, etc.), as well as reduced lung capacity. Greater patient anxiety increases the risk of complications, or even failure, (unexpected movement, stiffness, refusal to complete the procedure, etc.). In this study, music therapy using Music Care® tablets, was tested to replace EMONO. The study authors hypothesize that the use of the Music Care® device will have a comparable efficacy to that of EMONO (non-inferiority) in reducing patient anxiety during CT-guided lumbar infiltration. Furthermore, the study authors hypothesize that this simple, non-invasive method, with no contraindications for the patient, will be better tolerated and appreciated by both the patient and the paramedical team in charge of the treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * The patient must have given their free and informed consent and signed the consent form * The patient must be a member or beneficiary of a health insurance plan * Patients with low back pain for whom scan-guided infiltration is indicated, whether at the foraminal level, posterior joints, pudendal, epidural, sacroiliac, or via the sacrococcygeal hiatus. * Patient with an anxiety score ≥ 35/100 based on the STAI-ETAT questionnaire Exclusion Criteria: * The subject is participating in another drug or category I interventional study, or is in a period of exclusion determined by a previous study * The subject refuses to sign the consent * It is impossible to give the subject informed information * The patient is under safeguard of justice or state guardianship * Indication for epidural injection * Patient who is deaf or hard of hearing * Contraindications to EMONO * Facial or head trauma making it impossible to wear a nasofacial mask or headphones

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU de Nimes Nîmes France Recruiting

More Centre Hospitalier Universitaire de Nīmes trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06928740 on ClinicalTrials.gov ↗ ← All trials in France