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NCT01031550 · ClinicalTrials.gov registry record · NA
Isoflurane Preconditioning for Liver Resections
A NA study, sponsored by Rutgers, The State University of New Jersey.
- Terminated
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT01031550 is a NA study that was terminated before completion, run by Rutgers, The State University of New Jersey. The registered enrollment target is 8 participants.
The verdict
NCT01031550, a NA study, was terminated before completion, sponsored by Rutgers, The State University of New Jersey.
- TERMINATED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study Summary
The objective is to examine the efficacy of isoflurane (inhaled anesthetic gas) to induce clinically effective preconditioning in patients undergoing elective hepatic surgery.
Interventions
- DRUG propofol
- DRUG isoflurane
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2010-01 |
| Est. Completion | 2012-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01031550
The ClinicalTrials.gov registry entry for NCT01031550 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rutgers, The State University of New Jersey, which has 413 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which propofol is the first listed.
NCT01031550 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01031550 about?
NCT01031550 is a clinical study titled "Isoflurane Preconditioning for Liver Resections". The objective is to examine the efficacy of isoflurane (inhaled anesthetic gas) to induce clinically effective preconditioning in patients undergoing elective hepatic surgery.
What is the current status of trial NCT01031550?
This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2010-01. Estimated completion is 2012-06.
What interventions are being tested in trial NCT01031550?
The interventions under investigation include: propofol (DRUG), isoflurane (DRUG).
Who is sponsoring clinical trial NCT01031550?
This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.
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