Investigation of reported pain intensities and symptoms of stress in formerly ventilated internistic patients on intensive care unit – a prospective observational study
Recruiting
- Conditions
- R52.0Acute pain
- Registration Number
- DRKS00021112
- Lead Sponsor
- Zentrum für Palliativmedizin, Uniklinik Köln
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
patients that had to be ventilated artificially due to an internistic indication. Adult patients. Informed consent.
Exclusion Criteria
patients under 18 years. Missing informed consent. Chronic pain patients with ongoing opioid therapy. Delirium.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary endpoint: remembered pain intensity of patients during ventilation/ weaning; inquiry 2 - 6 days after Extubation with numeric rating scale
- Secondary Outcome Measures
Name Time Method -differences in pain intensity during the period of artificial ventilation with respect to aspects of opioid therapy <br>-symptoms of posttraumatic stress (PTSS-10) <br>-symptoms of depression (Depression, Anxiety and Stress Scale) <br>-satisfaction with pain therapy <br>-symptoms of delirium (CAM-ICU)<br>-quality of life (SF-12) <br>development of opioid-induced hyperalgesia/opioid tolerance (Quantitative Sensory Testing)<br><br>Data assessment: 2 - 6 days after extubation