Improving anesthesia outcomes with guided visualization for oral surgery patients
Does a Pre-sedation Guided Visualization Exercise Improve Outcomes in Ambulatory Anesthesia for Oral and Maxillofacial Surgery: a Double-blinded, Randomized Controlled Trial
This study tests if a short guided visualization exercise can improve the anesthesia experience for patients having oral surgery compared to those who only get standard instructions.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 8 Years to 70 Years |
| Sex | All |
| Sponsor | Alameda Health System Academic / other |
| Locations | 1 site (Oakland, California) |
| Trial ID | NCT06768021 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial evaluates the effectiveness of a brief guided visualization exercise on anesthesia-related outcomes in patients undergoing ambulatory anesthesia for oral and maxillofacial surgery. Participants will be divided into two groups: one receiving guided visualization along with standardized pre-operative instructions, and the other receiving only the standardized instructions. Key outcomes measured will include patient experience scores, sedation duration, medication usage, and recovery metrics. The goal is to determine if the addition of guided visualization can enhance the overall anesthesia experience.
Who should consider this trial
Good fit: Ideal candidates are patients aged 8 to 70 scheduled for ambulatory intravenous sedation in an oral and maxillofacial surgery clinic.
Not a fit: Patients who are not undergoing intravenous sedation or those with cognitive impairments or severe psychiatric conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved patient experiences and outcomes during anesthesia for oral and maxillofacial procedures.
How similar studies have performed: While the specific approach of guided visualization in this context may be novel, similar studies have shown positive outcomes with visualization techniques in other medical settings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subjects within ages 8 to 70. * Subjects planned for ambulatory intravenous sedation in the oral and maxillofacial surgery clinic. * Ability to understand verbal English or understand instructions using a sign-language or voice interpreter of their native language. Exclusion Criteria: * Subjects who cannot understand the instructions, even with an interpreter (extremes of age, cognitive impairments, severe psychiatric disease that may affect participation) * Subjects not undergoing intravenous sedation (oral sedation, nitrous oxide, local anesthesia) * Subjects undergoing anesthesia in other environments (gastrointestinal suite, operating rooms, interventional radiology)
Where this trial is running
Oakland, California
- Oral & Maxillofacial Surgery Clinic, Highland Hospital, Alameda Health System — Oakland, California, United States (Recruiting)
Study contacts
- Study coordinator: Omid Akramian, DMD
- Email: oakramian@alamedahealthsystem.org
- Phone: (510) 858-4007
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.