C56
Conditions
Interventions
Group 1: The anaesthesia records of patients who underwent surgery for ovarian cancer were retrospectively analysed to determine how much fluid they received intraoperatively. This fluid intake consis
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - cytoreductive tumour surgery
Exclusion criteria
Exclusion criteria: - final histology without evidence of ovarian carcinoma - Anaesthesia protocol not available
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the intraoperative fluid balance. It was determined in litres at the end of each operation and expressed as the difference between fluid input and fluid output. The fluid input was calculated on the basis of the volume information on the infusion solutions and blood products supplied, while the fluid output was determined by measuring the volume. | — |
Secondary
| Measure | Time frame |
|---|---|
| A secondary endpoint was the rate of postoperative complications that occurred during the postoperative stay. This information was taken (retrospectively) from the patient file. Another secondary endpoint was the survival rate at 1 year and 5 years after surgery. As part of the clinical routine, all patients and their general practitioners were contacted (independent of the study) regularly every 6 months and asked about their condition (and survival). This information and any date of death were noted in the medical records (independently of the study). For the study, this information was taken from the patient file. | — |
Countries
Germany
Contacts
Public ContactMartin Söhle
Universitätsklinikum Bonn
Outcome results
None listed