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NCT01195883 · ClinicalTrials.gov registry record · NA
Effect of Goal-directed Crystalloid Versus Colloid Administration on Major Postoperative Morbidity
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 1,102
- Enrollment target
NCT01195883 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 1,102 participants.
The verdict
NCT01195883, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,102 participants
- Enrollment target
Study Summary
A trial in which patients having open abdominal surgery are randomized to receive either crystalloids or colloids intraoperatively, guided by esophageal Doppler. The investigators test the primary hypothesis that goal-directed colloid administration during elective abdominal surgery decreases a composite of postoperative complications within 30 days of surgery.
Interventions
- DRUG Crystalloid
- DRUG Colloid
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,102 participants |
| Start Date | 2010-11 |
| Est. Completion | 2017-10-20 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01195883
The ClinicalTrials.gov registry entry for NCT01195883 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,102 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 Crystalloid is the first listed.
NCT01195883 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01195883 about?
NCT01195883 is a clinical study titled "Effect of Goal-directed Crystalloid Versus Colloid Administration on Major Postoperative Morbidity". A trial in which patients having open abdominal surgery are randomized to receive either crystalloids or colloids intraoperatively, guided by esophageal Doppler. The investigators test the primary hypothesis that goal-directed colloid administration during elective abdominal surgery decreases a comp...
What is the current status of trial NCT01195883?
This trial is currently completed. It is a NA study. The enrollment target is 1,102 participants. The study started on 2010-11. Estimated completion is 2017-10-20.
What interventions are being tested in trial NCT01195883?
The interventions under investigation include: Crystalloid (DRUG), Colloid (DRUG).
Who is sponsoring clinical trial NCT01195883?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
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