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NCT07219069: BIMV

Bispectral Monitoring on Mechanically Ventilated Patients

Not yet recruiting NA Last updated 21 October 2025
What this trial tests

NA trial testing BIS group in Sedation in 30 participants. Not yet recruiting.

Timeline
1 November 2025
Primary endpoint
1 November 2026
1 November 2026

Quick facts

Lead sponsorThe University of Texas Health Science Center, Houston
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment30
Start date1 November 2025
Primary completion1 November 2026
Estimated completion1 November 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

The University of Texas Health Science Center, Houston

Who can join

18 and older, any sex, with Sedation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine the difference in the duration of mechanical ventilation, to evaluate the difference in ICU length of stay and to determine the difference in the overall dose of sedation medications between the between participants who were monitored using Bispectral index monitoring (BIS) monitors and those who were not.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Sedation

Currently open trials in the same condition.

Other The University of Texas Health Science Center, Houston trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07219069.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing