Current Evidence Involving WALANT Surgery.
Katherine M Connors, Sara M Guerra, Steven M Koehler
https://pubmed.ncbi.nlm.nih.gov/36420465Actively Recruiting
Led by University of California, Irvine · Updated on 2026-03-12
134
Participants Needed
1
Research Sites
13 weeks
Total Duration
This research aims to determine whether eating solid food before a wide-awake local-only no tourniquet (WALANT) procedure affects patient anxiety and other outcomes. The study compares patients who eat before the procedure to those who fast, evaluating anxiety, nausea, satisfaction, and other measures. Researchers hypothesize that eating before the procedure will reduce anxiety and nausea and improve satisfaction compared to fasting. Participants are randomly assigned to either a fasting group, instructed to avoid food after midnight and liquids 4 hours before surgery, or an eating group, told to consume a light meal within two hours before their procedure. All patients undergo the WALANT procedure with standard preoperative care. Follow-up visits occur at 2 and 6 weeks post-procedure, with additional monitoring for complications up to 6 months. During the study, participants provide demographic information and complete assessments including the Amsterdam Preoperative Anxiety and Information Score, pain and nausea scales, and the QuickDASH questionnaire. Vital signs such as heart rate and blood pressure are collected before and after surgery. Satisfaction is measured at the first postoperative visit. Complications are tracked from medical records without extra procedures after the second visit.
CONDITIONS
Effect of Fasting on Patient Outcomes After Wide-Awake, Local Anesthesia-only, No Tourniquet (WALANT) Procedures
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or phone)
Duration - Day of procedure
Participants undergo their assigned fasting or eating protocol before their local anesthesia-only, no tourniquet procedure and then have the procedure performed.
1 visit (in-person, day of surgery)
Duration - 6 weeks
Participants are followed at 2 weeks and 6 weeks after their procedure to assess surgical satisfaction and arm function.
2 visits (approximately 2 weeks and 6 weeks post-procedure)
Total: 1 location
1
UCI Health Manchester Pavilion
Orange, California, United States, 92868
Actively Recruiting
M
Michael W Madsen, BA
M
Mikhail Pakvasa, MD
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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