Effect of establishing standardized, individually adapted pain therapy versus pattern-free pain therapy to reduce acute postoperative pain after ophthalmic surgery (such as enucleation, orbitotomy, or keratoplasty) - a prospective observational study
Recruiting
- Conditions
- C69Malignant neoplasm of eye and adnexa
- Registration Number
- DRKS00013995
- Lead Sponsor
- Zentrum für Palliativmedizin der Uniklinik Koeln
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 500
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
- 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
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method -Pain severity: measured with numeric rating scale (0 = no pain, 10 = maximum pain) on each postoperative day (and preoperative to exclude chronic pain)
- Secondary Outcome Measures
Name Time Method -Quality of life: obtained via SF36 questionnaire pre-surgery und on the 3rd day post-surgery<br>-Content with the pain-treatment: obtained via Quips-questionnaire on the 3rd day post-surgery<br>- (Additional ) medication use: amount of given non-narcotic-analgesics und opioids, obtained on the 1st -3rd day post-surgery <br>-Mortality: obtained on the 1st -3rd day post-surgery<br>-Morbidity: obtained on the 1st -3rd day post-surgery<br>-Therapy-induced adverse affects: obtained on the 1st -3rd day post-surgery<br>-Perioperative complications: obtained on the 1st -3rd day post-surgery<br>