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Validation of Aspiration Risk Assessment in Stroke Units

NCT06162910 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2024-02-05

No results posted yet for this study

Summary

The purpose of the study is to test the validity of a modified Daniels swallow test. The original test serves as reference method, the swallow endoscopy (FEES) as "gold standard".

Furthermore, it will be examined whether the modified Daniels test can be performed by nursing staff. As a reference method, the test will be performed by experienced speech therapists and the swallowing endoscopy (FEES) by speech therapists and/or physicians.

Conditions

  • Stroke, Acute

Interventions

DIAGNOSTIC_TEST

Daniels Water Swallow Test

Clinical water swallow dysphagia screening

DIAGNOSTIC_TEST

Flexible Endoscopic Evaluation of Swallowing

Endoscopic evaluation of swallowing function

Sponsors & Collaborators

  • University of Giessen

    lead OTHER

Principal Investigators

  • Samra Hamzic, PhD · University Hospital Giessen and Marburg, Campus Giessen

  • Tobias Braun, MD · University Hospital Giessen and Marburg, Campus Giessen

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-01
Primary Completion
2023-02-28
Completion
2023-02-28

Countries

  • Germany

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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 NCT06162910 on ClinicalTrials.gov