Topical Pharyngeal Anesthesia With Articaine for Gastroscopy

Sponsor
Helsinki University Central Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01350050
Collaborator
(none)
18
1
2
3
6

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Topical Pharyngeal anesthesia (TPA) is widely used as an adjunct to sedation during upper endoscopy. TPA improves patient tolerance and the ease of endoscopy.1 Methemoglobinemia and anaphylactic reactions are serious complications of such topical anaesthetic agents, as lidocaine, tetracaine, and benzocaine. Articaine is as a unique amide local anaesthetic that possesses both an amide and an ester linkage and this is of clinical significance in minimizing the risk of overdose (toxic reaction). In routine dental procedures, articaine is a superior anaesthetic to lidocaine. Also, in comparison to lidocaine articaine acts faster and its duration of action is shorter what may be an advantage in such relatively fast procedures as gastroscopy. Articaine have not been previously evaluated in pharyngeal anesthesia for upper endoscopy. The aim of this randomised double-blind placebo controlled study was to compare pharyngeal anesthesia with 4% articaine to placebo (Na0,9%) during gastroscopy in terms of benefit on patients' and endoscopists'satisfaction.

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Topical Pharyngeal Anaesthesia With Articaine for Gastroscopy. A Randomized Double-blind Study on Volunteers
Study Start Date :
Sep 1, 2009
Actual Primary Completion Date :
Dec 1, 2009
Actual Study Completion Date :
Dec 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: articaine

Pharyngeal anesthesia with articaine 4% or placebo should randomly and double-blindly applied in turns for every volunteer. In details: 3 ml of Articaine 4%solution or placebo (NaCl 0,9%) will be sprayed into the pharynx 5 minutes before beginning of gastroscopy. Also gastroscope will be lubricated with articaine (or placebo) gel(prepared by adding 4% articaine or 0,9%NaCl in placebo grope to Endopurin® endoscopic lubricant at the day of study).

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 Names:
  • Septocaine
  • Articadent
  • Placebo Comparator: placebo

    Pharyngeal anesthesia with placebo or articaine 4% should be randomly and double-blindly applied in turns for every volunteer. In details: 3 ml of placebo or Articaine 4% solution should be sprayed into the pharynx 5 minutes before beginning of gastroscopy. Also gastroscope will be lubricated with placebo(or articaine) gel(prepared by adding 4% articaine or 0,9%NaCl in placebo grope to Endopurin® endoscopic lubricant at the day of study).

    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.
    Other Names:
  • NaCl 0.9%
  • Outcome Measures

    Primary Outcome Measures

    1. satisfaction with gastroscopy [one day]

      Volunteers were asked to evaluate unpleasantness of gastroscopy (0- most unpleasant, 10-most pleasant), overall satisfaction with gastroscopy (0-extremely dissatisfied 7-extremely satisfied)

    Secondary Outcome Measures

    1. vital signs [one day]

      Vital signs (heart rate, electrocardiogram, non-invasive blood pressure, peripheral oxygen saturation, end-expiratory carbon dioxide) will be monitored during the gastroscopy and until the discharge.

    2. easiness of gastroscopy performance [one day]

      The easiness of gastroscopy performance will be evaluated by endoscopists' with structured questionnaire.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • healthy volunteers
    Exclusion Criteria:
    • pregnancy

    • allergy to articaine, propofol, alfentanil

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Helsiki University Central Hospital,Meilahti Hospital,Endoscopy unit Helsinki Uusimaa Finland 00029

    Sponsors and Collaborators

    • Helsinki University Central Hospital

    Investigators

    • Principal Investigator: Maxim Mazanikov, MD, Helsinki University Central Hospital,Department of Anesthesiology and Intensive Care
    • Study Director: Reino pöyhiä, MD,PhD, Helsinki University Central Hospital,Department of Anesthesiology and Intensive Care
    • Principal Investigator: Marianne Udd, MD,PhD, Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
    • Principal Investigator: Jorma Halttunen, MD,PhD, Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
    • Principal Investigator: Leena Kylänpää, MD,PhD, Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
    • Principal Investigator: Outi Lindström, MD,PhD, Helsinki University Central Hospital,Department of Gastrointestinal and General Surgery
    • Principal Investigator: Martti Färkkilä, MD,Professor, Helsinki University Central Hospital,Department of Medicine, Division of Gastroenterology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Maxim Mazanikov, M.D., Helsinki University Central Hospital
    ClinicalTrials.gov Identifier:
    NCT01350050
    Other Study ID Numbers:
    • a003c
    • 2009-011618-12
    First Posted:
    May 9, 2011
    Last Update Posted:
    Jul 6, 2012
    Last Verified:
    Jul 1, 2012
    Keywords provided by Maxim Mazanikov, M.D., Helsinki University Central Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 6, 2012