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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: Recruiting NA study of Surgery and Anesthesia, Local, sponsored by University of California, Irvine.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Measure of anxiety
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 |
What NCT05819801 shows while recruiting
NCT05819801 is an interventional study that assigns participants to a tested intervention. The registered 134 participants enrollment target is mid-sized for trials with a published cap, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Surgery
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.
Where NCT05819801's enrollment target sits among peer trials
134 50th of 120 higher than 71 of 120 other Surgery trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Surgery trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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