At a glance
ClinicalIndex Comparison RecordN/ACompleted· 321 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of the Effect of APFEL Risk Score and Fasting Periods on Postoperative Nausea and/or Vomiting
In Brief
An observational study for Nausea, Postoperative and 2 related conditions. Completed, enrolled 321 participants across 1 site.
Detailed Summary
This study, it is aimed to determine the effect of Apfel risk score and fasting times on postoperative nausea and vomiting (PONV).
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesTurkey (Türkiye)
CollaboratorsTarsus University
Timeline
N/ACompletedFinished
202420252026
Enrollment StartAug 2023
First PostedSep 2023
Primary CompletionApr 2024
Study CompletionAug 2024
TodayJul 2026
First PostedSep 5, 2023
Enrollment StartAug 28, 2023
Primary CompletionApr 5, 2024
Study CompletionAug 20, 2024
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 2.8 years ago