Fluid Management After Surgery in the Post-Anesthetic Care Unit (PACU)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.

Verified July 2009 by Shaare Zedek Medical Center.
Recruitment status was: Not yet recruiting

Sponsor:

Information provided by:

Shaare Zedek Medical Center

ClinicalTrials.gov Identifier:

NCT00947401

First received: July 26, 2009

Last updated: July 27, 2009

Last verified: July 2009

History of Changes

Purpose

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.

Condition
Surgery


Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Prospective
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

Resource links provided by NLM:

MedlinePlus related topics: Anesthesia

U.S. FDA Resources

Further study details as provided by Shaare Zedek Medical Center:


Estimated Enrollment:	1000
Study Start Date:	September 2009
Estimated Study Completion Date:	December 2010
Estimated Primary Completion Date:	June 2010 (Final data collection date for primary outcome measure)

Groups/Cohorts
elective post surgery patients

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.

Eligibility


Ages Eligible for Study:	18 Years and older (Adult, Senior)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

Adult patients (age > 18 yrs) after elective surgery

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

Contacts and Locations

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00947401

Contacts


Contact: Yaacov Gozal, MD	972-2-6555614	gozaly@szmc.org.il

Locations


Israel
Shaare Zedek Medical Center	Not yet recruiting
Jerusalem, Israel, 91031
Contact: Yaacov Gozal, MD 972-2-6555614 gozaly@szmc.org.il
Sub-Investigator: Sarah Shapira, RN

Sponsors and Collaborators

Shaare Zedek Medical Center

Investigators


Principal Investigator:	Yaacov Gozal, MD	Shaare Zedek Medical Center
Principal Investigator:	Sarah Shapira, RN	Shaare Zedek Medical Center

More Information


Responsible Party:	Yaacov Gozal, MD, Dept. of Anesthesiology, Shaare Zedek Medical Center, Jerusalem, Israel
ClinicalTrials.gov Identifier:	NCT00947401 History of Changes
Other Study ID Numbers:	1234567
Study First Received:	July 26, 2009
Last Updated:	July 27, 2009

Keywords provided by Shaare Zedek Medical Center:


Surgery, elective Fluids Post Anesthesia Care Unit PACU Fluid management

Additional relevant MeSH terms:


Anesthetics Central Nervous System Depressants Physiological Effects of Drugs

ClinicalTrials.gov processed this record on July 21, 2017

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