Effect of establishing a standardized, individually adapted pain therapy to reduce acute postoperative pain in ophthalmic surgery - a prospective observational study
- Conditions
- H57.1Ocular pain
- Registration Number
- DRKS00030059
- Lead Sponsor
- niversitätsklinikum KölnKlinik für Anästhesiologie und Operative Intensivemdizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 350
Inclusion Criteria
Patients undergoing orbitotomy, enucleation of the eye, corneal transplantation or other eye surgery
Minimum age 18 years
Present, signed informed consent form
Patient consent after detailed information about the study
ASA classification I-III
50 - 120 kg body weight
Exclusion Criteria
Intolerance to ibuprofen, metamizole, tilidine, tramadol, oxycodone, or morphine
Patients under 18 years of age
Patients who have not signed a consent form
Patients who could not be adequately informed due to language and comprehension problems.
Patients who were not cleared for surgery after the premedication visit due to their pre-existing conditions released for surgery
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint of this observational study is pain severity reported on all postoperative days and at discharge.
- Secondary Outcome Measures
Name Time Method Secondary endpoints are quality of life, (additional) analgesic consumption, adverse events, mortality, morbidity, and perioperative complications, e.g., wound healing disorders.