Music, Anesthetic, Induction
Conditions
Brief summary
Anesthetic induction requires the use of, among other things, hypnotic drugs that can lead to hemodynamic disorders, postoperative cognitive dysfunctions and delayed awakening. A strategy to reduce the doses of hypnotics administered could improve patients' postoperative outcomes and is part of the current strategy of accelerated postoperative rehabilitation. Music has shown its effectiveness in reducing the doses of hypnotics administered during sedation procedures. Objective : We propose a study of this anesthetic period evaluating the effectiveness of music as an adjuvant agent for anesthetic drugs allowing hypnotic savings. Materials and methods : Randomized, prospective, monocentric study 2 groups will be compared. The experimental group will benefit from musical listening during the induction period of the anesthesia. The control group will have a usual care. The primary endpoint is the amount of hypnotic (propofol®) used during anesthesia induction. The main secondary criteria are the duration of induction, the cost of induction, and the postoperative pain score and the proportion of patients with postoperative nausea and vomiting. This study should include 104 subjects (52 in each group) requiring general anesthesia. Hypothesis tested: Listening to music reduces the amount of hypnotic product used in the induction of anesthesia by 0.5 mg/kg.
Interventions
OTHERmusic
listening music
Sponsors
University Hospital, Caen
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Intervention model description
2 groups will be compared. The experimental group will benefit from musical listening during the induction period of the anesthesia. The control group will have a usual care.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient presenting for surgery under general anesthesia in ophthalmic surgery, ENT, CMF and neurosurgery (lumbar and cervical disc hernia, neurostimulator insertion, vertebral cementoplasty) * Score ASA 1, 2, 3. * Intervention time \< 3 hours.
Exclusion criteria
* Patients under 18 years of age * Patient under guardianship or curatorship * Refusal of the patient * Deaf patient * Non-cooperating patient * Anesthetic protocol different from that standardised
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| quantity of propofol | 2 months | quantity of propofol in mg/kg necessary for the induction of general anaesthesia |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Quantity of morphinomimetics | 2 months | Quantity of morphinomimetics (morphine equivalent) used in mg for anesthetic induction. |
Countries
France
Outcome results
None listed