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PACU Discharge Without Motorfunction Assessment After Spinal Anaesthesia

Primary Purpose

Osteoarthritis Susceptibility 3

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
assessment of motorfunction in PACU
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis Susceptibility 3 focused on measuring hip, knee, arthroplasty, spinal, anesthesia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 18 yr or more
  • primary unilateral total hip or knee arthroplasty
  • spinal anesthesia

Exclusion Criteria:

  • intraoperative conversion to general anesthesia
  • intraoperative bleeding exceeding 750 ml.

Sites / Locations

  • Gentofte Hospital
  • Vejle Sygehus
  • Farsø Sygehus
  • Holstebro Sygehus
  • Viborg Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

no assessment of motorfunction in PACU

motorfunction assessment in PACU

Arm Description

no assessment of motorfunction after spinal anesthesia in PACU

Assesment of motorfunction after spinal anesthesia

Outcomes

Primary Outcome Measures

Lenght of stay (in days) or 30 day readmissions
The main outcome is a compund measure of the duration of hospitalization after operation )measured in days, and named Length of Stay LOS) adn/or re-admission within the first 30 days after discharge.

Secondary Outcome Measures

Adverse events
Any event that results in a physicians assessment of the patient, not including regular rounds during the first 24 hours after surgery.

Full Information

First Posted
April 28, 2014
Last Updated
November 24, 2016
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT02134496
Brief Title
PACU Discharge Without Motorfunction Assessment After Spinal Anaesthesia
Official Title
PACU Discharge Without Motorfunction Assessment After Spinal Anaesthesia for Total Hip or Knee Arthroplasty - a Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
June 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study investigates the safety of discharge from the Post-Anesthesia Care Unit (PACU) without assessment of motorfunction after spinal anesthesia for total hip- or knee replacement. This is an randomized controlled trial between two groups with assessment of normal (Aldrete) PACU discharge criteria with or without assessment of the motorfunction. The study hypothesis is that it is safe to be discharged from the PACU to a ward without assessment of motor function. The main outcome is length of hospial stay (LOS) in days and re-admission within the first 30 days after surgery . Secondary outcomes include adverse events up to 24 hours after surgery, and minuttes spent in the PACU after surgery. Participants will be monitores for adverse events for the first 24 hours after surgery and reported. The total number of minuttes spent in the PACU will be recorded and reported.
Detailed Description
A novel analysis of the latest database version was performed 06.04.2015, showing that 86.7% of patients have LOS of less than 5 days and no re-admission within the first 30 days after discharge. The study is designed as a non-inferiority study with a two-sided 5% significance level, 80% power and a non-inferiority level of 5%, resulting in 2 x 725 patients (1500 in total including drop-outs). A 30-day re-admission period was chosen to detect complications that could be assumed to have occurred as a consequence of the potential earlier PACU discharge The study will also investigate Length of stay, incidence of failed anesthesia, and reason for stay in PACU after THA and TKA 24.11.2016 A substudy based upon the un-published data from the time in PACU will be performed to analyse factors related to adverse events occuring during the PACU stay, and description of specific organdysfunction based upon the recordings from the modifed Aldrete discharge criteria. Preoperative demographic data are collected from charts and the Lundbeck Centre for Fast-track Hip and Knee Replacement database, (LCDB), intraoperative data from anesthesia charts. A logistic regression analysis will be performed with the YES/NO outcome of moderate/severe adverse PACU events at any time during PACU stay, and pre- and intr operatie variables.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis Susceptibility 3
Keywords
hip, knee, arthroplasty, spinal, anesthesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1511 (Actual)

8. Arms, Groups, and Interventions

Arm Title
no assessment of motorfunction in PACU
Arm Type
No Intervention
Arm Description
no assessment of motorfunction after spinal anesthesia in PACU
Arm Title
motorfunction assessment in PACU
Arm Type
Active Comparator
Arm Description
Assesment of motorfunction after spinal anesthesia
Intervention Type
Procedure
Intervention Name(s)
assessment of motorfunction in PACU
Intervention Description
assessment of motorfunction in PACU after spinal anesthesia
Primary Outcome Measure Information:
Title
Lenght of stay (in days) or 30 day readmissions
Description
The main outcome is a compund measure of the duration of hospitalization after operation )measured in days, and named Length of Stay LOS) adn/or re-admission within the first 30 days after discharge.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Adverse events
Description
Any event that results in a physicians assessment of the patient, not including regular rounds during the first 24 hours after surgery.
Time Frame
24 hours postooperatively
Other Pre-specified Outcome Measures:
Title
Time to discharge from PACU
Description
Time from arrival to discharge i PACU measured in minuttes
Time Frame
12 hours
Title
Discharge readiness before leaving the operating theater
Description
How many patients fulfilled the PACU discahrge criteria at the time they were leaving the operating theater
Time Frame
1 hour
Title
Failed spinal anesthesia.
Description
Incidence and related factors to failed spinal anesthesia (ie. conversion to generel anesthesia)
Time Frame
6 hours.
Title
Prediction of PACU complications
Description
Factors related to, and incidence of, moderate/severe complications i PACU
Time Frame
0-7 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18 yr or more primary unilateral total hip or knee arthroplasty spinal anesthesia Exclusion Criteria: intraoperative conversion to general anesthesia intraoperative bleeding exceeding 750 ml.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henrik Kehlet, Professor
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Eske K Aasvang, M.D., DMSci
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gentofte Hospital
City
Gentofte
State/Province
International
ZIP/Postal Code
2900
Country
Denmark
Facility Name
Vejle Sygehus
City
Vejle
State/Province
International
ZIP/Postal Code
7100
Country
Denmark
Facility Name
Farsø Sygehus
City
Farsø
ZIP/Postal Code
4640
Country
Denmark
Facility Name
Holstebro Sygehus
City
Holstebro
Country
Denmark
Facility Name
Viborg Hospital
City
Viborg
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
29578248
Citation
Aasvang EK, Laursen MB, Madsen J, Kroigaard M, Solgaard S, Kjaersgaard-Andersen P, Mandoe H, Hansen TB, Nielsen JU, Krarup N, Skott AE, Kehlet H. Incidence and related factors for intraoperative failed spinal anaesthesia for lower limb arthroplasty. Acta Anaesthesiol Scand. 2018 Aug;62(7):993-1000. doi: 10.1111/aas.13118. Epub 2018 Mar 26.
Results Reference
derived

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PACU Discharge Without Motorfunction Assessment After Spinal Anaesthesia

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