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Recovery at the Post Anaesthetic Care Unit After Hip and Knee Arthroplasty

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01178489
First Posted: August 10, 2010
Last Update Posted: September 22, 2011
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.
Information provided by (Responsible Party):
Troels Haxholdt Lunn, Hvidovre University Hospital
August 9, 2010
August 10, 2010
September 22, 2011
August 2010
January 2011   (Final data collection date for primary outcome measure)
Time to meet PACU discharge criteria [ Time Frame: 3 hours ]
Not Provided
Complete list of historical versions of study NCT01178489 on ClinicalTrials.gov Archive Site
  • Actual discharge time from PACU [ Time Frame: 3 hours ]
  • Clinical and logistic factors detaining patients in PACU [ Time Frame: 3 hours ]
  • Potential complications at the surgical ward [ Time Frame: 24 hours ]
Not Provided
Not Provided
Not Provided
 
Recovery at the Post Anaesthetic Care Unit After Hip and Knee Arthroplasty
Recovery at the Post Anaesthetic Care Unit After Fast-track Hip and Knee Arthroplasty
To clarify patient related problems in the Post Anaesthetic Care Unit (PACU) immediately after fast-track hip and knee arthroplasty.

In this prospective, consecutive, observational cohort study we examine:

  1. Patient related problems in the PACU after hip and knee arthroplasty simply to answer the question "Why in PACU?", using a modified version of the national guidelines for patient observation in PACU.
  2. The time spent in PACU with the modified version of the national guidelines for patient observation in PACU.
  3. If the modified version of the national guidelines for patient observation in PACU results in patient related problems in the ward afterwards.
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Probability Sample
Patients undergoing primary, unilateral, total hip or knee arthroplasty
  • PACU Stay After THA Under Spinal Anaesthesia
  • PACU Stay After TKA Under Spinal Anaesthesia
Not Provided
Patients undergoing arthroplasty
Patients undergoing primary, unilateral, total hip or knee arthroplasty under spinal anaesthesia
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
170
January 2011
January 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • primary, unilateral, total hip or knee arthroplasty by one of three surgeons using the same technique, and under spinal anaesthesia

Exclusion Criteria:

  • Bilateral arthroplasty
  • Revision arthroplasty
  • General anaesthesia
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
 
NCT01178489
H-1-2010-FSP
No
Not Provided
Not Provided
Troels Haxholdt Lunn, Hvidovre University Hospital
Hvidovre University Hospital
Not Provided
Principal Investigator: Troels H Lunn, M.D. Hvidovre University Hospital
Hvidovre University Hospital
September 2011
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