R10-R19 R10.0 R10.1 R10.2 R10.3 R10.4
Conditions
Interventions
Group 1: Intervention group: Patients with atraumatic abdominal pain from the start of the APU intervention
Group 2: Control group: Patients with atraumatic abdominal pain from the start of the projec
Sponsors
Notfall- und Akutmedizin,Charité - Universitätsmedizin Berlin, Campus Charité Mitte und Campus Virchow-Klinikum (CCM/CVK) (C-Not)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adult patients with atraumatic abdominal pain and ability to give consent (by themselves or their caregivers)
Exclusion criteria
Exclusion criteria: Obvious trauma or accident as cause of abdominal pain
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acute pain on leaving the emergency room, patient satisfaction, duration of emergency room care | — |
Secondary
| Measure | Time frame |
|---|---|
| Process evaluation, Quality improvement, Health Economics | — |
Countries
Germany
Contacts
Public ContactMartin Möckel
Notfall- und Akutmedizin,Charité - Universitätsmedizin Berlin, Campus Charité Mitte und Campus Virchow-Klinikum (CCM/CVK) (C-Not)
Outcome results
None listed