Evaluation of an Analgosedation Protocol in Mechanically Ventilated Patients

Withdrawn before enrolling · Not applicable

Conditions studied: Effect of Protocolized Sedation on Days of Mechanical Ventilation in the ICU

In brief

The purpose of this study is to evaluate how the investigators provide sedation (medicine that make you sleepy) in the investigators intensive care unit (ICU). This study will look at a new way of using sedation in the ICU to see what effect it has on patients and if it decreases the amount of time spent on mechanical ventilation (machine that breathes for you), and in the ICU.

Key facts

Study ID

NCT02100735

Run by

Tampa General Hospital

People needed

0

Starts

2019-09-13

Expected to finish

2021-04-01

Last updated by the study team

2020-10-19

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients 18 years of age and older
• Patients expected to require mechanical ventilation for greater than 48 hrs

You may not qualify if…

• Need for continuous neuromuscular blockade
• Severe chronic neurocognitive dysfunction
• Tracheostomy at the time of study enrollment
• Alcohol withdrawal risk or symptoms
• Drug overdose
• Chronic use of narcotics
• Active seizures

Where it is running

• Beatrice Adams — Riverview, Florida, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.