Randomized clinical trial of the optimization of procedural pain control in ICU patients
Phase 4
Completed
- Conditions
- Patiënten op de ICU, zowel electief als niet electief opgenomenpain relief
- Registration Number
- NL-OMON31005
- Lead Sponsor
- Sint Antonius Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
Patients admitted to the ICU of the St. Antonius hospital, with the age of 18 years or older.
Exclusion Criteria
- Pregnancy/ breastfeeding
- Language barrier
- Known morphine allergy
- Comatose patient (cooled)
- Patients who are suspected to be braindead
- Unintubated patients on the verge of intubation due to respiratory
insufficiency
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The percentage of patients with a NRS of >= 4 during intervention (2.5 mg versus<br /><br>7.5 mg morphine)</p><br>
- Secondary Outcome Measures
Name Time Method