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Perioperative Relevance of Intraoperative Anuric Episodes Within a Goal-directed Haemodynamic Algorithm in Patients Undergoing Laparotomy Due to Epithelial Ovarian Cancer


N/A
18 Years
N/A
Not Enrolling
Female
Intraoperative Anuria

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Trial Information

Perioperative Relevance of Intraoperative Anuric Episodes Within a Goal-directed Haemodynamic Algorithm in Patients Undergoing Laparotomy Due to Epithelial Ovarian Cancer


Inclusion Criteria:



- Offered patient information and written informed consent

- Female patients aged greater than or equal to 18 years for cytoreductive surgery of a
primary epithelial ovarian tumour

Exclusion Criteria:

- Patients with relapse Ovarian Cancer

- Patients aged less than 18 years

- Persons without the capacity to consent

- Unability of German language use

- Lacking willingness to save and hand out data within the study

- Accommodation in an institution due to an official or judicial order

- (Unclear) history of alcohol or substances disabuse

- Coworker of the Charité

- Advanced disease of the oesophagus or upper respiratory tract at the beginning of
hospitalisation

- Operation in the area of the oesophagus or nasopharynx within the last two months
before participation in the study

- Neurological or psychiatric disease at the beginning of hospitalisation

- CHF (congestive heart failure) according to (New York Heart Association)
classification - NYHA class IV at the beginning of hospitalisation

- American Society of Anaesthesiologists (ASA) classification greater than IV

- Renal insufficiency (dependency of haemodialysis) at the beginning of hospitalisation

- Pulmonal oedema in thorax x-ray at the beginning of hospitalisation

- History of intracranial hemorrhage within one year before participation in the study

- Conditions following venous thrombosis within the last three years before study
inclusion

- Known allergies or hypersensitivity on colloidal, starch or gelatine infusion
solutions

- Diabetes mellitus with signs of severe neuropathy

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Exact measurement of urine production

Outcome Description:

Exact measurement of urine production (number of anuric episodes anf duration of anuric episodes in minutes)

Outcome Time Frame:

During the operation and in the 72-hour postoperative sample period

Safety Issue:

No

Authority:

Germany: Ethics Commission

Study ID:

EPERIA

NCT ID:

NCT01703442

Start Date:

October 2013

Completion Date:

February 2015

Related Keywords:

  • Intraoperative Anuria
  • Anuria

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