Topical Pharyngeal Anesthesia With Articaine for Gastroscopy
NCT01350050 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 18
Last updated 2012-07-06
Summary
Topical Pharyngeal anesthesia (TPA) is widely used during upper endoscopy. Articaine is local anaesthetic that have not been previously evaluated in pharyngeal anesthesia for upper endoscopy. The aim of this study was to compare pharyngeal anesthesia with 4% articaine to placebo (Na0,9%) during gastroscopy in terms of benefit on patients' and endoscopists' satisfaction.
Conditions
- Gastroscopy
Interventions
- DRUG
-
articaine
Articaine is intermediate-acting local anesthetic (amide type). Like other local anesthetic drugs, articaine causes a transient and completely reversible state of anesthesia (loss of sensation) during (dental) procedures. In dentistry, articaine is used both for infiltration and block injections.
- OTHER
-
9% Sodium Chloride solution for injection
9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer.
Sponsors & Collaborators
-
Helsinki University Central Hospital
lead OTHER
Principal Investigators
-
Maxim Mazanikov, MD · Helsinki University Central Hospital,Department of Anesthesiology and Intensive Care
-
Reino pöyhiä, MD,PhD · Helsinki University Central Hospital,Department of Anesthesiology and Intensive Care
-
Marianne Udd, MD,PhD · Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
-
Jorma Halttunen, MD,PhD · Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
-
Leena Kylänpää, MD,PhD · Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
-
Outi Lindström, MD,PhD · Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
-
Martti Färkkilä, MD,Professor · Helsinki University Central Hospital,Department of Medicine, Division of Gastroenterology
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-09-30
- Primary Completion
- 2009-12-31
- Completion
- 2009-12-31
Countries
- Finland
Study Locations
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