T88.5
Conditions
Interventions
Group 1: (intervention group): Patients receive ice to reduce postoperative pain and nausea
Group 2: (control group 1): Patients receive unsweetened tea/coffee
Group 3: (control group 2): Patients rec
Sponsors
Klinik für Anästhesiologie und operative Intensivmedizin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -Plastic surgery and trauma surgery patients who are undergoing elective surgery. surgery -Adult patients over the age of 18 -Consent to participate in the study (written)
Exclusion criteria
Exclusion criteria: - Patients with chronic pain lasting longer than 3 months - Addiction patients (especially substance addiction) - Patients who have undergone outpatient surgery - Cognitively impaired patients, e.g. with dementia or other cognitive disorders -Patients with current psychotropic drug therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is the frequency and severity of post-operative nausea and vomiting (PONV) in the recovery room, measured using a standardised PONV score (e.g. Nausea and Vomiting Index) within the first hours after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Analgesic requirements in the recovery room: Total amount and type of pain medication administered for post-operative pain treatment. Antiemetic requirement: Need for antiemetic medication to treat nausea and vomiting in the recovery room. Pain intensity: Subjective pain assessment by patients using the Numerical Rating Scale (NRS) from 0-10. Postoperative well-being: Survey of the patient's subjective well-being using a standardised, short patient questionnaire in the recovery room (e.g. scale or questionnaire - optional depending on protocol design). | — |
Countries
Germany
Contacts
Public ContactJerome Defosse
Klinik für Anästhesiologie und operative Intensivmedizin
Outcome results
None listed