AduLt iatrogEnic withdRawal sTudy in the ICU (ALERT-ICU)

NCT04422808 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2437

Last updated 2022-07-29

No results posted yet for this study

Summary

Withdrawal from opioids and sedatives administered for medical purposes (i.e. iatrogenic withdrawal) often goes unrecognized in the critically ill, but its prevalence is high. Reports describing what is being implemented at the bedside to prevent iatrogenic withdrawal are lacking, and how patients are monitored and assessed for withdrawal has not been adequately studied. Therefore, the investigators overall objective is to determine the current analgesia and sedation weaning practices in adult ICUs. In order to accomplish this objective the investigators plan to conduct a prospective, observational, point prevalence trial. Data from this project will help support future investigation of iatrogenic withdrawal.

Conditions

  • Withdrawal Syndrome
  • Iatrogenic Disease

Sponsors & Collaborators

  • Wilkes University

    lead OTHER

Principal Investigators

  • Gilles L Fraser, PharmD, MCCM · Tufts University School of Medicine

  • Scott Bolesta, PharmD, BCPS · Wilkes University

  • Marc M Perreault, MSc, PharmD · Université de Montréal

  • Lisa Burry, PharmD · MOUNT SINAI HOSPITAL

  • Brian L Erstad, PharmD, MCCM · The University of Arizona College of Pharmacy

  • Céline Gélinas, N., Ph.D. · Ingram School of Nursing

  • Richard R Riker, MD, FCCM · Tufts University School of Medicine

  • Katrianna D Saltarelli, Student · Wilkes University

  • Jennifer Mitchell, Student · Wilkes University

  • Kathryn E Smith, PharmD, BCPS, BCCCP · MaineHealth

  • Federico Carini, MD · Hospital Italiano de Buenos Aires

  • Rebekah Eadie, MPharm, MSc, IP, MPSNI · Ulster Hospital- South Eastern Health and Social Care Board

  • Jamie Harpel, Student · Wilkes University

  • Ryan Stewart, Student · Wilkes University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-01
Primary Completion
2021-09-30
Completion
2022-04-01

Countries

  • United States

Study Locations

More Related Trials

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 NCT04422808 on ClinicalTrials.gov