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NCT01563991 · ClinicalTrials.gov registry record · NA
Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 186
- Enrollment target
NCT01563991 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 186 participants.
The verdict
NCT01563991, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 186 participants
- Enrollment target
Study 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.
Interventions
- PROCEDURE Normal fluid volume
- PROCEDURE Reduced fluid volume
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 186 participants |
| Start Date | 2007-02 |
| Est. Completion | 2012-04-18 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01563991
The ClinicalTrials.gov registry entry for NCT01563991 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 186 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Normal fluid volume is the first listed.
NCT01563991 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01563991 about?
NCT01563991 is a clinical study titled "Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes". 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.
What is the current status of trial NCT01563991?
This trial is currently completed. It is a NA study. The enrollment target is 186 participants. The study started on 2007-02. Estimated completion is 2012-04-18.
What interventions are being tested in trial NCT01563991?
The interventions under investigation include: Normal fluid volume (PROCEDURE), Reduced fluid volume (PROCEDURE).
Who is sponsoring clinical trial NCT01563991?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
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