Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04408911
Other study ID # RetroLoveMi
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2006
Est. completion date December 31, 2018

Study information

Verified date May 2020
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this retrospective cohort study is to evaluate the effect of lormetazepam versus midazolam on hospital mortality, intensive care unit outcomes and sedation management.

The hypothesis is that patients receiving midazolam have a 5% higher hospital mortality in comparison to patients receiving lormetazepam.


Description:

Sedation is an integral part of modern intensive care medicine and has seen a tremendous development throughout the last years. Current guideline recommendations are targeted at an awake critically ill patients (target Richmond Agitation-Sedation Scale 0/-1) as early deep sedation has been shown to negatively affect the outcome. Nevertheless, is an adequate and individualized anxiolysis still an important intervention that can be achieved via process optimization, modifications to the infrastructure of the ward and pharmacologic therapy. Bolus application of benzodiazepines is a recommended pharmacologic measure to achieve proper anxiolysis. Midazolam is currently the most commonly used benzodiazepine in European intensive care units. Midazolam accumulates after repetitive application due to its pharmacokinetic properties, which increases the likelihood for side effects and makes targeted sedation increasingly difficult. Lormetazepam is used with increasing frequency as it is eliminated independent of the patients age and has few relevant metabolites. It is therefore thought to be better suited for targeted sedation management, which in turn would be beneficial for the patients.

The aim of this retrospective cohort study is to evaluate the effect of lormetazepam versus midazolam on hospital mortality, intensive care unit outcomes and sedation management.


Recruitment information / eligibility

Status Completed
Enrollment 3314
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Intensive care unit patients at the Charité - Universitätsmedizin Berlin

- Age = 18 years

- Intensive care unit length of stay = 48 hours

- Duration of mechanical ventilation > 0 hours

- Midazolam or lormetazepam application during the ICU stay

Exclusion Criteria:

- Number of application < 2

- Midazolam and lormetazepam application during the intensive care unit stay

- Neurosurgical intensive care unit patients

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Midazolam vs. Lormetazepam
In this retrospective analysis we compared critically ill ICU patients receiving midazolam to those receiving lormetazepam.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Charite University, Berlin, Germany

Outcome

Type Measure Description Time frame Safety issue
Primary Hospital Mortality Proportion of patients that between hospital admission and hospital discharge On average 20 days, for each study subject measured up to study completion day 12-31-2018
Secondary Incidence of delirium during the intensive care unit stay Incidence of delirium diagnosed on the intensive care unit On average 7 days, for each study subject measured up to study completion day 12-31-2018
Secondary Duration of delirium during the intensive care unit stay Duration patients had a delirium on the intensive care unit On average 3 days, for each study subject measured up to study completion day 12-31-2018
Secondary Hospital length of stay Time patients spend admitted to the hospital On average 30 days, for each study subject measured up to study completion day 12-31-2018
Secondary Intensive care unit length of stay Time patients spend admitted to the intensive care unit On average 7 days, for each study subject measured up to study completion day 12-31-2018
Secondary Duration of mechanical ventilation Time patients are mechanically ventilated On average 4 days, for each study subject measured up to study completion day 12-31-2018
See also
  Status Clinical Trial Phase
Completed NCT04551508 - Delirium Screening 3 Methods Study
Recruiting NCT06037928 - Plasma Sodium and Sodium Administration in the ICU
Completed NCT03671447 - Enhanced Recovery After Intensive Care (ERIC) N/A
Recruiting NCT03941002 - Continuous Evaluation of Diaphragm Function N/A
Recruiting NCT04674657 - Does Extra-Corporeal Membrane Oxygenation Alter Antiinfectives Therapy Pharmacokinetics in Critically Ill Patients
Completed NCT04239209 - Effect of Intensivist Communication on Surrogate Prognosis Interpretation N/A
Completed NCT05531305 - Longitudinal Changes in Muscle Mass After Intensive Care N/A
Terminated NCT03335124 - The Effect of Vitamin C, Thiamine and Hydrocortisone on Clinical Course and Outcome in Patients With Severe Sepsis and Septic Shock Phase 4
Completed NCT02916004 - The Use of Nociception Flexion Reflex and Pupillary Dilatation Reflex in ICU Patients. N/A
Recruiting NCT05883137 - High-flow Nasal Oxygenation for Apnoeic Oxygenation During Intubation of the Critically Ill
Completed NCT04479254 - The Impact of IC-Guided Feeding Protocol on Clinical Outcomes in Critically Ill Patients (The IC-Study) N/A
Recruiting NCT04475666 - Replacing Protein Via Enteral Nutrition in Critically Ill Patients N/A
Not yet recruiting NCT04516395 - Optimizing Antibiotic Dosing Regimens for the Treatment of Infection Caused by Carbapenem Resistant Enterobacteriaceae N/A
Not yet recruiting NCT04538469 - Absent Visitors: The Wider Implications of COVID-19 on Non-COVID Cardiothoracic ICU Patients, Relatives and Staff
Withdrawn NCT04043091 - Coronary Angiography in Critically Ill Patients With Type II Myocardial Infarction N/A
Recruiting NCT02922998 - CD64 and Antibiotics in Human Sepsis N/A
Recruiting NCT02989051 - Fluid Restriction Keeps Children Dry Phase 2/Phase 3
Completed NCT03048487 - Protein Consumption in Critically Ill Patients
Completed NCT02899208 - Can an Actigraph be Used to Predict Physical Function in Intensive Care Patients? N/A
Recruiting NCT02163109 - Oxygen Consumption in Critical Illness