Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes (NCT01563991) | Clinical Trial Compass
CompletedNot Applicable
Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes
United States186 participantsStarted 2007-02
Plain-language summary
Subjects undergoing surgery on the small or large bowel will be randomized to one of 2 groups, a normal fluid amount group and a reduced fluid amount group to evaluate the impact of this change on recovery after surgery.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients 18 years or older
* ASA I-III
* Ability to provide informed consent
* Creatinine less than or equal to 1.3 mg/mL)
Exclusion Criteria:
Patients younger than 18 years old
* ASA IV or higher
* Urgent or emergent surgery
* Mental disease or addictive disorders impairing ability to provide informed consent
* Renal insufficiency (Cr greater than 1.3 mg/mL)
* Significant language barriers
* Cirrhosis causing ascites
* NYHA III or IV, EF less than 25%
* Use of intraoperative epidural anesthesia
* Uncontrolled diabetes
* Uncontrolled hypertension in the opinion of the enrolling surgeon
* ETOH consumption greater than 35 drinks weekly
* Cachexia or absolute neutrophil count of less than 1,200/mm3
* Existing uncontrolled coagulopathy or platelet count of less than 100,000/mm3