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Evaluation of the persistency of the preoperative anxiolytic effect of music therapy vs midazolam: electroencephalographic and clinical analysis
EU CTIS ID: 2025-522575-29-00
What this study is testing
To evaluate the persistence of the preoperative anxiolytic effect of music therapy versus midazolam using electroencephalographic and clinical analysis.
- Therapeutic use (Phase IV)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- Patients who have been scheduled for surgery and have agreed to give informed consent for the study.
You likely can't join if
- Refusal to be part of the study on a voluntary basis
- Patients who report dissatisfaction with music therapy
- Severe hearing loss
- A patient condition that impairs the ability to comprehend the study information.
- A history of allergic reactions to benzodiazepines
- Conditions in which benzodiazepine use is not recommended, such as severe obstructive apnea, morbid obesity, or other relevant conditions considered by an anesthesiologist.
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.