Post Anesthesia Care Unit Length of StayNCT01826292
The Association Between Anesthetic and Surgical Practices and Patient Length of Stay in the Post Anesthesia Care Unit
An observational study of Post Anesthesia Care Unit Length of Stay, run by University of California, Davis.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Post Anesthesia Care Unit Length of Stay
- How many people
- 0 participants
- Where
- No sites listed yet
- Study dates
- Nov 2012to Nov 2015
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
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.
Who may be able to join
- 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.
Who cannot join
- Patients less than 18-years of age,
- Patients transferred to the intensive care unit, and
- Patients for whom data is not reported.
About this study
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.
Read the 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.
- Conditions
- Post Anesthesia Care Unit Length of Stay
- Keywords
- Post anesthesia care unit length of stay
What is being measured
The primary outcome is the main question the study is designed to answer.
Patient length of stay in the post anesthesia care unit
Measured: Three months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Apr 2013 (estimated)
- Study startNov 2012
- Primary completionNov 2015
- Study completionNov 2015
Why it stopped: Principle Investigator was not able to proceed with the study
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Post Anesthesia Care Unit Length of StayStudies of the same condition, open and under way.
- More trials run by University of California, DavisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Retrospective
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of California, Davis
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Harmeet Bhullar, MD, Principal investigator, University of California, Davis
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01826292
- Sponsor's protocol ID
- 363700
- Status last verified
- Apr 2017
- First submitted
- 3 Apr 2013
- Last updated
- 19 Apr 2017
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Apr 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Association Between Anesthetic and Surgical Practices and Patient Length of Stay in the Post Anesthesia Care Unit
- ClinicalTrials.gov ID
- NCT01826292
- Acronym / sponsor ID
- 363700
- Conditions
- Post Anesthesia Care Unit Length of Stay
- Keywords
- Post anesthesia care unit length of stay
- Study type
- Observational
- Recruitment status
- WithdrawnReason stopped: Principle Investigator was not able to proceed with the study
- Enrolment
- 0 participants (actual)
- Lead sponsor
- University of California, DavisUniversity, hospital or other
- Study start
- Nov 2012
- Primary completion
- Nov 2015 (actual)
- Study completion
- Nov 2015 (actual)
- First posted
- 8 Apr 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Observational model
- Other
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- 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.
Key inclusion criteria (1 listed)
- 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.
Key exclusion criteria (3 listed)
- Patients less than 18-years of age,
- Patients transferred to the intensive care unit, and
- Patients for whom data is not reported.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Patient length of stay in the post anesthesia care unit
Time frame: Three months
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Apr 2017.
Related trials for Post Anesthesia Care Unit Length of Stay
Not yet recruitingObservational study
Comparison of IV Dexmedetomidine Versus Clonidine Versus no Alpha 2 Agonist on Emergency Delirium, PACU Length of Stay and Time to Hospital Discharge in Children Undergoing (Adeno)Tonsillectomy: a Prospective Observational Study
Emergency Delirium, Postoperative Delirium (POD)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Harmeet Bhullar, MD principal investigator
University of California, Davis
Questions about this trial
What is this clinical trial studying?
An observational study of Post Anesthesia Care Unit Length of Stay, run by University of California, Davis.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: withdrawn, as of the sponsor's last update on 19 Apr 2017. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Patient length of stay in the post anesthesia care unit (time frame: Three months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Apr 2017.