Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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: Completed NA study, sponsored by The Cleveland Clinic.
NCT01195883 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 1,102 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (22% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Any of the following major complications: (1) Cardiac (Acute heart failure/Myocardial infarction/Ventricular arrhythmia); (2) pulmonary (embolism/edema/respiratory failure/pneumonia/pleural effusion); (3) gastrointestinal (bowel and surgical anastomosis stricture or anastomotic leak/internal or external fistulas/peritoneal effusions); (4) Renal (requiring dialysis); (5) Infectious (deep or organ space surgical site infection / sepsis); and (6) Coagulation (bleeding).
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 |
What the finished NCT01195883 record still lists
NCT01195883 is an interventional study that assigns participants to a tested intervention. Its 1,102 participants enrollment target places it among the larger protocols in the corpus, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (22% lower).
The record links to 0 conditions, and to 2 interventions - of which Crystalloid is the first listed.
NCT01195883 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01195883's enrollment target sits among peer trials
1,102 93rd of 2000 higher than 1,908 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00710112 · 1,100 participants
Genetic Variants and Susceptibility to Diseases of Prematurity in Very Low Birth-Weight Infants
- NCT02688517 · 1,100 participants
Targeted Genomic Analysis of Blood and Tissue Samples From Patients With Cancer
- NCT04743765 · 1,100 participants · NA
HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 Trial
- NCT05638581 · 1,100 participants · Phase 3
Trauma Resuscitation With Low-Titer Group O Whole Blood or Products
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia