RecruitingNot Applicable

Evaluation of the Impact of Virtual Reality on Sedation Use in Patients Undergoing Regional Anesthesia for Scheduled Orthopedic Surgery

France164 participantsStarted 2024-07-18

Plain-language summary

The VIRTUALR study evaluates the effect of virtual reality combined with hypnosis on anxiety in patients undergoing orthopedic surgery under regional anesthesia. Patients are randomly assigned to two groups: one group receiving virtual reality and a control group without the device. Anxiety and satisfaction questionnaires are used to compare the two groups.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Signed informed consent * Patient affiliated with or benefiting from a social security system * Patient aged 18 years or older * Patient requiring regional anesthesia for scheduled orthopedic surgery of the upper or lower limb Exclusion Criteria: * Patient refusal to participate in the study * Device interfering with the surgical or anesthetic procedure * Premedication before arrival in the operating room * Psychiatric or cognitive disorders, communication disorders * Patient unable to understand the study (language barrier, psychological issues) * Emergency surgery

What they're measuring

Comparison of sedation use rates between the experimental group and the control group (level 0 versus ≥1).

Timeframe: Intraoperative period (from arrival in the operating room to the end of surgery)

Trial details

NCT IDNCT07013695

SponsorCentre Hospitalier Eure-Seine

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-07-17

Contact for this trial

Lydia BEN BEKKOU

02 32 33 86 75 arc2.circe@ch-eureseine.fr

View on ClinicalTrials.gov More Orthopedic Procedure trials