The purpose of this study is to examine in prospective, double-blinded randomised manner the ability of novel articaine-containing lozenge to enhance the procedure related compliance (compared to placebo) of the adult patients undergoing upper gastrointestinal endoscopy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
120
Department of Anesthesiology and Intensive care medicine, Divison of Surgery, Meilahti hospital, Helsinki University Central Hospital
Helsinki, Uusimaa, Finland
RECRUITINGPercentage of participants with 15% change in tolerability points according to Numeric Rating Scale (compared to baseline Numeric Rating Scale).
Time frame: 30 minutes after the procedure
Endoscopists´ procedural satisfaction points after the procedure assessed by using Numeric Rating Scale (NRS)
Time frame: within 30 minutes after the procedure
Cumulative consumption of alfentanil during the procedure (mg)
Time frame: 30 minutes after the procedure
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