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New treatment option for Procedural Sedation
Official title Personalized Music, Dreaming During Propofol Sedation
ClinicalTrials.gov ID: NCT07638072
What this study is testing
- What it's testing
- This randomized clinical trial will evaluate whether music delivered through closed-back headphones during intravenous propofol sedation affects dreaming and the overall sedation experience. Adults scheduled for elective procedures under spinal anesthesia or peripheral nerve block with propofol sedation will be randomly assigned to one of three groups: patient-selected preferred music, matched non-preferred music, or silence with identical headphones.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 19 and older. Healthy volunteers may be eligible.
You may be able to join if
- Adults aged 19 years or older.
- Scheduled to undergo an elective procedure under spinal anesthesia or peripheral nerve block with intravenous propofol sedation.
- American Society of Anesthesiologists physical status I to III.
- Able to provide written informed consent.
- Able to wear closed-back headphones during the study period.
You likely can't join if
- Planned general anesthesia.
- Severe hearing impairment that would interfere with the auditory intervention.
- Major psychiatric instability or condition that may interfere with study participation or dream assessment.
- Expected significant intraoperative bleeding.
- Inability to complete the required postoperative interviews or questionnaires.
- Contraindication to propofol or other study sedative agents.
See the full eligibility criteria
- Adults aged 19 years or older.
- Scheduled to undergo an elective procedure under spinal anesthesia or peripheral nerve block with intravenous propofol sedation.
- American Society of Anesthesiologists physical status I to III.
- Able to provide written informed consent.
- Able to wear closed-back headphones during the study period.
- Able to complete postoperative interviews and study questionnaires.
- Planned general anesthesia.
- Severe hearing impairment that would interfere with the auditory intervention.
- Major psychiatric instability or condition that may interfere with study participation or dream assessment.
- Expected significant intraoperative bleeding.
- Inability to complete the required postoperative interviews or questionnaires.
- Contraindication to propofol or other study sedative agents.
- Refusal or withdrawal of informed consent.
The study team makes the final eligibility decision.
Where it's taking place
- Iksan, Jeollabukdo, South Korea
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, 19 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Iksan, Jeollabukdo, South Korea. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.