Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06768021 · ClinicalTrials.gov registry record · NA
Does Style of Pre-sedation Instructions Improve Patient Outcomes in Ambulatory Anesthesia for Oral and Maxillofacial Surgery?
A NA study of Anesthesia Complication and Anesthesia Recovery Period, sponsored by Alameda Health System.
- Recruiting
- Registry status
- NA
- Development phase
- 300
- Enrollment target
- 1
- Study location
NCT06768021 is a NA study of Anesthesia Complication and Anesthesia Recovery Period that is actively recruiting participants, run by Alameda Health System. The registered enrollment target is 300 participants, below the 3,400-participant average among 4 other Anesthesia Complication trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06768021, a NA study of Anesthesia Complication and Anesthesia Recovery Period, is actively recruiting participants, sponsored by Alameda Health System.
- RECRUITING
- Registry status
- NA
- Development phase
- 300 participants
- Enrollment target
- 1
- Study location
Study Summary
This randomized controlled trial aims to evaluate the impact of a brief guided visualization exercise on anesthesia-related outcomes in oral and maxillofacial surgery in patients scheduled for ambulatory anesthesia in the oral and maxillofacial surgery clinic. Researchers will compare these patients, who will receive the guided visualization exercise in addition to standardized pre-operative instructions, to patients who will only receive the standardized pre-operative instructions. The following outcomes will be measured for both groups: * A seven-point Anesthesia Experience Survey * Face-Legs-Activity-Cry-Consolability (FLACC) scores at three points in time during the anesthetic - during local anesthesia, during surgery, and fifteen minutes after surgery has concluded * Amount of medications used during the sedation * Length of sedation
Conditions Studied
Interventions
- BEHAVIORAL Guided visualization and standardized pre-sedation instructions
- BEHAVIORAL Standardized pre-sedation instructions only
Study Locations (1)
California
- Oral & Maxillofacial Surgery Clinic, Highland Hospital, Alameda Health System - Oakland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2025-01-02 |
| Est. Completion | 2026-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06768021
The ClinicalTrials.gov registry entry for NCT06768021 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,400-participant average among 4 other Anesthesia Complication trials with a reported enrollment target (91% lower). The listed sponsor is Alameda Health System, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 6 conditions, with Anesthesia Complication appearing as the primary indexed condition, and to 2 interventions - of which Guided visualization and standardized pre-sedation instructions is the first listed.
NCT06768021 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06768021 about?
NCT06768021 is a clinical study titled "Does Style of Pre-sedation Instructions Improve Patient Outcomes in Ambulatory Anesthesia for Oral and Maxillofacial Surgery?". This randomized controlled trial aims to evaluate the impact of a brief guided visualization exercise on anesthesia-related outcomes in oral and maxillofacial surgery in patients scheduled for ambulatory anesthesia in the oral and maxillofacial surgery clinic. Researchers will compare these patients...
What is the current status of trial NCT06768021?
This trial is currently recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2025-01-02. Estimated completion is 2026-06.
What conditions does trial NCT06768021 study?
This clinical trial studies the following conditions: Anesthesia Complication, Anesthesia Recovery Period, Anesthesia, Intravenous, Anesthesia Induction, Anesthesia Outcomes.
What interventions are being tested in trial NCT06768021?
The interventions under investigation include: Guided visualization and standardized pre-sedation instructions (BEHAVIORAL), Standardized pre-sedation instructions only (BEHAVIORAL).
Who is sponsoring clinical trial NCT06768021?
This trial is sponsored by Alameda Health System, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06768021 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Anesthesia Complication
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
RECRUITING · NA
-
Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial)
RECRUITING · Phase 3
-
Arm and Ankle Blood Pressure Cuffs During C-Section
COMPLETED
-
Perioperative Complications of Deep Extubation in Adults
COMPLETED
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.