TerminatedNot Applicable

Prevalence of Preoperative Dehydration in Major Elective Urologic Surgery and Its Impact on Postoperative Outcome

Stopped: Due to COVID-19 study inclusion was halted on March 16, 2020 after 309 days.

Switzerland188 participantsStarted 2019-02-12

Plain-language summary

The primary objective of this study is to measure the prevalence of preoperative dehydration in elective major abdominal urologic surgery when we apply our daily standard operation procedures. Secondary objectives are to assess the impact of preoperative dehydration on postoperative outcome. The hypothesis is that preoperative dehydration leads to more postoperative complications.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * \>18 years old * Major elective urologic surgery i. Prostate surgery ii. Bladder surgery iii. Kidney surgery iv. Various laparotomies / laparoscopies (e.g. retroperitoneal lymphadenectomy) * Standard procedure planned * Standard perioperative management planned * Informed consent Exclusion Criteria: * Preoperative iv-fluids * Pregnancy (which is a contraindication to this type of surgery per se) * Inability to give informed consent (e.g. severe psychiatric disorder, dementia) * Inability to complete the Quality of Recovery (QoR) questionnaire * Enrolment of the investigator, his/her family members, employees and other dependent persons

What they're measuring

Prevalence of Dehydration at Induction of Anesthesia

Timeframe: Time point 0: time (estimated between 7am and 4pm on day of surgery) at Induction of Anesthesia for Major Urologic Surgery

Trial details

NCT IDNCT03788070

SponsorInsel Gruppe AG, University Hospital Bern

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-03-16

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