C69
Conditions
Interventions
Group 1: Oral pattern-free pain medication by the treating ward physician in 500 patients with eye surgery.
Sponsors
Zentrum für Palliativmedizin der Uniklinik Koeln
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Patients undergoing eye surgery - Present and signed informed consent - Patient’s consent, after having been informed in detail on the study - ASA Classification I-III - 50 – 120 kg bodyweight - Minimum age 18 years
Exclusion criteria
Exclusion criteria: - Intolerance to Ibuprofene, Metamizole, Tilidine, Oxycodon or Morphine - Pre-existing chronic pain - Patients, who haven’t signed informed consent - Patients younger than 18 years - Patients, who haven’t been approved for surgery due to their pre-existing conditions after the premedication visit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| -Pain severity: measured with numeric rating scale (0 = no pain, 10 = maximum pain) on each postoperative day (and preoperative to exclude chronic pain) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Quality of life: obtained via SF36 questionnaire pre-surgery und on the 3rd day post-surgery - Content with the pain-treatment: obtained via Quips-questionnaire on the 3rd day post-surgery - (Additional ) medication use: amount of given non-narcotic-analgesics und opioids, obtained on the 1st -3rd day post-surgery - Mortality: obtained on the 1st -3rd day post-surgery - Morbidity: obtained on the 1st -3rd day post-surgery - Therapy-induced adverse affects: obtained on the 1st -3rd day post-surgery - Perioperative complications: obtained on the 1st -3rd day post-surgery | — |
Countries
Germany
Contacts
Public ContactJohannes Loeser
Zentrum für Palliativmedizin der Uniklinik Koeln
Outcome results
None listed