Clinical trial · Interventional
Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes
Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes Following Elective Open Colorectal Surgery
NCT01563991CI-TRIAL-00026704completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Benign Neoplasm of Intestinal Tract | — | UNRESOLVED | — |
| Primary Malignant Neoplasm of Intestinal Tract | — | UNRESOLVED | — |
| Secondary Malignant Neoplasm of Intestinal Tract | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Normal fluid volume | Procedure | — | UNRESOLVED |
| Reduced fluid volume | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Standard fluid volume
- description
- Subject receives normal fluid volume during peri-operative period
- interventionNames
- Procedure: Normal fluid volume
- type
- EXPERIMENTAL
- label
- Reduced Fluid Volume
- description
- Subject receives a reduced fluid volume during the peri-operative period
- interventionNames
- Procedure: Reduced fluid volume
Primary outcomes (1)
- measure
- Morbidity
- timeFrame
- 5-7 days
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.