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Trial record 1 of 448 for:    shaare zedek
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Fluid Management After Surgery in the Post-Anesthetic Care Unit (PACU)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00947401
Recruitment Status : Unknown
Verified July 2009 by Shaare Zedek Medical Center.
Recruitment status was:  Not yet recruiting
First Posted : July 28, 2009
Last Update Posted : July 28, 2009
Sponsor:
Information provided by:
Shaare Zedek Medical Center

Tracking Information
First Submitted Date July 26, 2009
First Posted Date July 28, 2009
Last Update Posted Date July 28, 2009
Study Start Date September 2009
Estimated Primary Completion Date June 2010   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History No Changes Posted
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Fluid Management After Surgery in the Post-Anesthetic Care Unit (PACU)
Official Title 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
Brief Summary 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.
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
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Adult patients (age > 18 yrs) after elective surgery
Condition Surgery
Intervention Not Provided
Study Groups/Cohorts elective post surgery patients
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Unknown status
Estimated Enrollment
 (submitted: July¬†27,¬†2009)
1000
Original Estimated Enrollment Same as current
Estimated Study Completion Date December 2010
Estimated Primary Completion Date June 2010   (Final data collection date for primary outcome measure)
Eligibility Criteria

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
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Israel
Removed Location Countries  
 
Administrative Information
NCT Number NCT00947401
Other Study ID Numbers 1234567
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Yaacov Gozal, MD, Dept. of Anesthesiology, Shaare Zedek Medical Center, Jerusalem, Israel
Study Sponsor Shaare Zedek Medical Center
Collaborators Not Provided
Investigators
Principal Investigator: Yaacov Gozal, MD Shaare Zedek Medical Center
Principal Investigator: Sarah Shapira, RN Shaare Zedek Medical Center
PRS Account Shaare Zedek Medical Center
Verification Date July 2009