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Transnasal and Oral Gastroscopy.

NCT00273117 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2006-01-09

No results posted yet for this study

Summary

Two groups of patients were randomised into two groups of either transnasal gastroscopy or conventional type gastroscopy (n=98). The aim of the study was to evaluate the cardiorespiratory effects and sideeffects of the two methods, and to evaluate the technical features of the transnasal endoscope.

Conditions

  • Upper Gastrointestinal Disease, Duodenal or Gastric Ulcer.

Interventions

PROCEDURE

transnasal gastroscopy

Sponsors & Collaborators

  • Glostrup University Hospital, Copenhagen

    collaborator OTHER

  • Hvidovre University Hospital

    lead OTHER

Principal Investigators

  • Merete Christensen, MD · Dept. of Cardiothoracic Surgery, Copenhagen University Hospital Rigshospitalet, Denmark

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-02-28
Completion
2003-08-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00273117 on ClinicalTrials.gov