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NCT05819801 · ClinicalTrials.gov registry record · NA
Effect of Fasting on Patient Outcomes After Wide-Awake, Local Anesthesia-only, No Tourniquet (WALANT) Procedures
A NA study of Surgery and Anesthesia, Local, sponsored by University of California, Irvine.
- Recruiting
- Registry status
- NA
- Development phase
- 134
- Enrollment target
- 1
- Study location
NCT05819801 is a NA study of Surgery and Anesthesia, Local that is actively recruiting participants, run by University of California, Irvine. The registered enrollment target is 134 participants, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05819801, a NA study of Surgery and Anesthesia, Local, is actively recruiting participants, sponsored by University of California, Irvine.
- RECRUITING
- Registry status
- NA
- Development phase
- 134 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine whether eating solid food prior to undergoing a wide awake local-only no tourniquet (WALANT) procedure reduces anxiety in patients or has any effect on outcomes. Patients will be split randomly into two groups and told whether to eat or fast before their procedure. We will then compare levels of anxiety and nausea on the day of the procedure as well as satisfaction with the procedure and other outcome measures at follow-up visits. Our hypothesis is that patients who are instructed to eat before their WALANT procedure will have less anxiety, nausea, and overall higher satisfaction compared to those who are instructed to fast prior to their procedure.
Conditions Studied
Interventions
- OTHER Fasting
- OTHER Non-fasting
Study Locations (1)
California
- UCI Health Manchester Pavilion - Orange
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 134 participants |
| Start Date | 2024-02-22 |
| Est. Completion | 2026-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05819801
The ClinicalTrials.gov registry entry for NCT05819801 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 134 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The listed sponsor is University of California, Irvine, which has 368 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Surgery appearing as the primary indexed condition, and to 2 interventions - of which Fasting is the first listed.
NCT05819801 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT05819801 about?
NCT05819801 is a clinical study titled "Effect of Fasting on Patient Outcomes After Wide-Awake, Local Anesthesia-only, No Tourniquet (WALANT) Procedures". The purpose of this study is to determine whether eating solid food prior to undergoing a wide awake local-only no tourniquet (WALANT) procedure reduces anxiety in patients or has any effect on outcomes. Patients will be split randomly into two groups and told whether to eat or fast before their pro...
What is the current status of trial NCT05819801?
This trial is currently recruiting. It is a NA study. The enrollment target is 134 participants. The study started on 2024-02-22. Estimated completion is 2026-09.
What conditions does trial NCT05819801 study?
This clinical trial studies the following conditions: Surgery, Anesthesia, Local, Fasting.
What interventions are being tested in trial NCT05819801?
The interventions under investigation include: Fasting (OTHER), Non-fasting (OTHER).
Who is sponsoring clinical trial NCT05819801?
This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05819801 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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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.