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Valuation of Swallowing in Patient Sedated for Gastroenteric Endoscopic Procedure

NCT01789424 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2015-03-17

No results posted yet for this study

Summary

Aim of this study is to evaluate swallowing functionality in patient sedated for gastroenteric endoscopic procedure.

Swallowing will be study by laryngeal fibroscopy and evaluate using Penetration-Aspiration Scale and Aspiration Risk validated in scientific literature.

Aim of the study is to describe swallowing, as an expression of airway protection, in sedated patient. in particular, our purpose is to determine the incidence of moderate-severe and severe swallowing alteration (level 3 or 4 of Aspiration Risk scale).

Conditions

  • Sedation for Gastroenteric Endoscopic Procedure
  • Deglutition Disorders
  • Aspiration of Food

Sponsors & Collaborators

  • Ospedale San Raffaele

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2013-05-31
Completion
2013-12-31

Countries

  • Italy

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 NCT01789424 on ClinicalTrials.gov