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Clinical Trials/NCT01134133
NCT01134133WithdrawnPhase 1

Can Hospital Acquired Pneumonia be Prevented in Patients Who Gurgle?

Bridgeport Hospital0 sites50 target enrollmentStarted: February 1, 2010Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Withdrawn
Enrollment
50
Primary Endpoint
Hospital acquired pneumonia

Study Overview

Brief Summary

Hospital inpatients who have gurgling sounds heard during speech or breathing have been observed to have a higher risk of hospital acquired pneumonia. Patients who gurgle and who consent to participation will be randomized to receive routine clinical management or management to include measures employed to reduce risks of aspiration, namely, 1. head of bed up (30 degrees or higher), 2. swallowing evaluation by speech therapist (and feeding predicated on formal evaluation), 3. prompting managing physicians to reduce sedating medications to minimal effective dose.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Gurglers who consent to participate

Exclusion Criteria

  • Non-gurglers
  • Patients presenting with pneumonia prior to identification with gurgling
  • Patients receiving comfort-care-only

Outcomes

Primary Outcomes

Hospital acquired pneumonia

Time Frame: 14 days (average)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

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