- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00947401
Fluid Management After Surgery in the Post-Anesthetic Care Unit (PACU)
July 27, 2009 updated by: Shaare Zedek Medical Center
The Practice of Fluid Management in the Post-anesthetic Care Unit (PACU) of Shaare Zedek Medical Center in Patients Undergoing Elective Surgery: an Observational Study
The objective of the present study is to describe the current practice of postoperative fluid management in the Post Anesthesia Care Unit (PACU) of the Shaare Zedek Medical Center, Jerusalem, Israel.
Study Overview
Status
Unknown
Conditions
Detailed Description
The aim of this study is to follow and present the current practice of fluid administration in the PACUof Shaare Zedek Medical Center for an extended period of time as a first step towards establishing guidelines for postoperative fluid management.
Study Type
Observational
Enrollment (Anticipated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Jerusalem, Israel, 91031
- Shaare Zedek Medical Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adult patients (age > 18 yrs) after elective surgery
Description
Inclusion Criteria:
- age > 18 yrs
- elective surgery
- ASA I-III
Exclusion Criteria:
- massive intraoperative blood loss
- non elective surgery
- pregnant women
- stay in the PACU < 15 minutes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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elective post surgery patients
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yaacov Gozal, MD, Shaare Zedek Medical Center
- Principal Investigator: Sarah Shapira, RN, Shaare Zedek Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2009
Primary Completion (Anticipated)
June 1, 2010
Study Completion (Anticipated)
December 1, 2010
Study Registration Dates
First Submitted
July 26, 2009
First Submitted That Met QC Criteria
July 27, 2009
First Posted (Estimate)
July 28, 2009
Study Record Updates
Last Update Posted (Estimate)
July 28, 2009
Last Update Submitted That Met QC Criteria
July 27, 2009
Last Verified
July 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- 1234567
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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