NCT03487510

Brief Summary

Recording of routine practice patterns to detect and/or treat Dysphagia on the ICU via interview of local colleagues. This will not allow to record generalizable data, but will reflect the actual routine standard of care.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
49

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 11, 2017

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

March 9, 2018

Completed
26 days until next milestone

First Posted

Study publicly available on registry

April 4, 2018

Completed
27 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2018

Completed
Last Updated

November 12, 2024

Status Verified

May 1, 2018

Enrollment Period

6 months

First QC Date

March 9, 2018

Last Update Submit

November 7, 2024

Conditions

Deglutition Disorders

Keywords

treatment standardsdiagnostical approachesdescriptive

Outcome Measures

Primary Outcomes (1)

  • Number of centers using fibre-optic endoscopic evaluation of swallowing (FEES) vs. non-instrumental methods to detect/ treat dysphagia on the ICU.

    Analysis of number of ICUs using instrumental methods (FEES) vs. non-instrumental methods in local (Swiss) centers to detect dysphagia in the ICU.

    through study completion, an average of 1 month

Study Arms (1)

NO groups

no groups apply.

Other: NO interventions apply

Interventions

NO interventions applyOTHER

does not apply

NO groups

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Senior local ICU physicians (Swiss ICUs only).

You may qualify if:

  • All senior ICU physicians in charge for adult critically ill ICU patients. Respective ICUs must be accredited by the "Schweizerische Gesellschaft für Intensivmedizin".
  • ICUs located in Switzerland.
  • Senior ICU physicians willing to voluntarily fill in the provided questionnaire.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dept. of Intensive Care Medicine, University of Bern,

Bern, 3010, Switzerland

Location

MeSH Terms

Conditions

Deglutition Disorders

Condition Hierarchy (Ancestors)

Esophageal DiseasesGastrointestinal DiseasesDigestive System DiseasesPharyngeal DiseasesOtorhinolaryngologic Diseases

Study Officials

  • Patrick Zürcher, MD

    Inselspital, University of Bern

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Sponsor-investigator

Study Record Dates

First Submitted

March 9, 2018

First Posted

April 4, 2018

Study Start

November 11, 2017

Primary Completion

May 1, 2018

Study Completion

May 1, 2018

Last Updated

November 12, 2024

Record last verified: 2018-05

Data Sharing

IPD Sharing
Will not share

Locations

CH(1)