- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01826292
The Association Between Anesthetic and Surgical Practices and Patient Length of Stay in the Post Anesthesia Care Unit
April 17, 2017 updated by: University of California, Davis
The investigators are conducting a retrospective, cross-sectional chart review of patients who underwent an anesthetic administered by an anesthesiologist in the University of California Davis main operating rooms and were transferred to the main post anesthesia care unit between January 1, 2012 and March 31, 2012.
The investigators are excluding patients less than 18 years of age, patients transferred to the intensive care unit, and patients for whom data is not reported.
Our aim is to report the incidences patient characteristics, as well as anesthetic and surgical techniques, and the associations these factors may have with the outcome of patient length of stay in the PACU.
Study Overview
Status
Withdrawn
Conditions
Detailed Description
We are conducting a retrospective, cross-sectional chart review of patients who underwent an anesthetic administered by an anesthesiologist in the University of California Davis main operating rooms and were transferred to the main (Pavilion) post anesthesia care unit between January 1, 2012 and March 31, 2012.
We are excluding patients less than 18-years of age, patients transferred to the intensive care unit, and patients for whom data is not reported.
Charts will be reviewed and data will be collected by the primary and co-investigator(s).
Analysis will consist of cross-tabulation counts across independent variables, univariate analysis (outcome variable PACU length of stay), and regression analysis (outcome variable PACU length of stay).
We aim to measure patient length of stay in the post anesthesia care unit (PACU) as the outcome variable.
The following patient, operative, and post operative factors will be recorded as covariates: age, gender, height, weight, American Society of Anesthesiologists physical status classification, pre-operative use of pain medication, pre-operative pain score, whether the patient is non-English speaking, history of smoking, surgical service, anesthetic time, surgical time, urgency of surgery, use of general anesthetic or monitored anesthesia care, use of regional anesthetic, regional anesthetic type, use of inhalational or total intravenous anesthetic maintenance, intraoperative use of dexmedetomidine, intraoperative use of dexamethasone, intraoperative use of ondansetron, intraoperative use of remifentanyl, intraoperative use of ketamine, total volume of crystalloid or colloid administered, intraoperative use of endotracheal tube, natural airway, or laryngeal mask airway, time of PACU arrival, initial pain score in the PACU, episode of post operative nausea or vomiting, administration of antiemetic in the PACU, post operative temperature, time of anesthesiologist sign out in the PACU, time of patient transfer from the PACU, location of transfer from PACU, preoperative placement of scopolamine patch, history of postoperative nausea and vomiting, type of surgery (including categories of major abdominal-open, orthopedic, ear nose and throat, thoracic, vascular, ophthalmology, abdominal-laparoscopic, urology, minor, neurology, and plastics), intra operative estimated blood loss, intra operative administration of the following medications: dexamethasone, antiemetics including dexamethasone, acetaminophen, ketorolac, muscle relaxant (i.e.
paralytics), muscle relaxant reversal agents, and morphine equivalent dosage of opioids; intra operative volume of colloid administered, intra operative volume of blood products administered, morphine equivalent dosage of opioids administered in the post anesthesia care unit, times of admission and discharge from the post anesthesia care unit.
The data will be labeled with a code that the research team can link to personal identifying information when acquired.
The code sheet will be secured and kept separate from the dataset.
The primary and co-investigator(s) will be the only individuals who have access to the password protected database stored on a secure server at the University of California Davis Medical Center.
Study Type
Observational
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
Patients who underwent an anesthetic administered by an anesthesiologist in the University of California Davis main operating rooms and were transferred to the main post anesthesia care unit between January 1, 2012 and March 31, 2012.
Description
Inclusion Criteria:
- Patients who underwent an anesthetic administered by an anesthesiologist in the University of California Davis main operating rooms and were transferred to the main post anesthesia care unit between January 1, 2012 and March 31, 2012.
Exclusion Criteria:
- Patients less than 18-years of age,
- Patients transferred to the intensive care unit, and
- Patients for whom data is not reported.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Patient length of stay in the post anesthesia care unit
Time Frame: Three months
|
Three months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Harmeet Bhullar, MD, University of California, Davis
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
November 1, 2012
Primary Completion (Actual)
November 1, 2015
Study Completion (Actual)
November 1, 2015
Study Registration Dates
First Submitted
April 3, 2013
First Submitted That Met QC Criteria
April 5, 2013
First Posted (Estimate)
April 8, 2013
Study Record Updates
Last Update Posted (Actual)
April 19, 2017
Last Update Submitted That Met QC Criteria
April 17, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 363700
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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