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Optimization of a Fast-track Concept for Knee Joint Replacement (KneeOptOut2)

Primary Purpose

Knee Arthropathy, Postoperative Pain, Postoperative Complications

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Late local infiltration analgesia
Early local infiltration analgesia
Sponsored by
Charite University, Berlin, Germany
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Arthropathy focused on measuring ERAS, pain, knee arthroplasty, joint pain, regional anaesthesia

Eligibility Criteria

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

Inclusion Criteria:

• patients undergoing elective, primary knee joint replacement in combined general anaesthesia

Exclusion Criteria:

  • heart insufficiency NYHA >2
  • liver insufficiency > CHILD B
  • evidence of diabetic polyneuropathy
  • severe adipositas BMI >40
  • patients < 18 years
  • pregnancy
  • in case of police custody
  • participation in a paralleled interventional RCT in a time frame of 30 days
  • chronic opioid therapy >3 months before scheduled surgery
  • allergy against medication required for surgery or anaesthesia

Sites / Locations

  • Charité - Universitätsmedizin Berlin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Early-intraoperative Local infiltration technique

Late-intraoperative Local infiltration technique

Arm Description

A distal regional anaesthesia is performed in which the nerves are blocked by a local anaesthetic in the tissue in the immediate vicinity of the operating area ("tissue infiltration technique"). The LIA is applied in a total of 4 steps during the preparation of the knee joint: 1. after the skin incision, 2. after the capsule incision, 3. after complete exposure of the knee joint, 4. when the posterior knee capsule is reached.

A distal regional anaesthesia is performed in which the nerves are blocked by a local anaesthetic in the tissue in the immediate vicinity of the operating area ("tissue infiltration technique"). The LIA is applied after the preparation of the femur and tibia bone shortly before the prosthesis is inserted and during the retreat from the knee joint.

Outcomes

Primary Outcome Measures

Opioid consumption
amount of opioids administered intraoperative measured as equivalent dose to morphin

Secondary Outcome Measures

time to first mobilisation (standing)
time from end of surgery until patients is able to stand
patients satisfaction (11-point likert scale)
global satisfaction of patients
time to first mobilisation (walking)
time from end of surgery until patients is able to walk
time to achieve full joint mobility
time to achieve full joint mobility (0/0/90°)
Janda grade of both legs at first day after surgery
best Janda grade in both legs the day after surgery
Pain intensity
intensity of pain in all patients meausered by numeric rating scale (NRS)
rescue pain medication
number of patients requiring rescue pain medication
time to discharge
time to discharge from hospital
Opioid consumption (hospital)
amount of opioids administered until discharge measured as equivalent dose to morphin
delirium
incidence of postoperative delirium measured by Nursing Delirium Screening Scale (NuDeSc)
postoperative nausea and vomiting (PONV)
incidence of PONV
surgeon satisfaction (6-point likert scale)
satisfaction of surgeon in points of clarity of the operative field, change of the operative field by LIA and overall satisfaction represented in one value

Full Information

First Posted
April 16, 2019
Last Updated
February 13, 2023
Sponsor
Charite University, Berlin, Germany
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1. Study Identification

Unique Protocol Identification Number
NCT03920930
Brief Title
Optimization of a Fast-track Concept for Knee Joint Replacement
Acronym
KneeOptOut2
Official Title
Optimization of a Fast-track Concept for Knee Replacement: A Single-blind, Randomized, Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2019 (Actual)
Primary Completion Date
February 28, 2021 (Actual)
Study Completion Date
July 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Charite University, Berlin, Germany

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In an estimated 150,000 patients, a knee joint replacement is performed in Germany every year. The perioperative care of the patients aims at an optimal surgical technique, which leads to a high functionality in the joint, and above all at an adequate pain treatment. Patients experience pain especially intraoperatively and in the first days after the operation. The intensity of pain is a decisive factor that can hinder the patient's mobilization. In the KneeOptOut study (ethics application number EA4/009/17), which has already been successfully carried out and approved by this ethics committee, it was shown that the use of local infiltration anaesthesia (LIA) for pain therapy after primary knee endoprosthetics is comparable to catheter-supported regional anaesthesia (manuscript under review at the European Journal of Anaesthesiology). During surgery, the morphine requirement of patients in the LIA group was significantly higher than that of patients who underwent catheterization. Postoperatively, however, both subjective pain by VAS and opiate consumption were comparable. In order to optimize the intraoperative opiate need/consumption, an early-intraoperative procedure for local infiltration anesthesia will now be compared with the previous late-intraoperative procedure. Both procedures correspond to SOP for the treatment of primary knee endoprostheses and are currently used depending on the surgeon's requirements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Arthropathy, Postoperative Pain, Postoperative Complications
Keywords
ERAS, pain, knee arthroplasty, joint pain, regional anaesthesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Investigator and treating physicians are different in this trial, that means, the assessor of primary study endpoint will be blinded regarding group allocation. Patients receive either early or late local infiltration technique perioperatively. Patients will be blinded against early or late local infiltration technique. Blinding of the treating physician will not be possible.
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early-intraoperative Local infiltration technique
Arm Type
Experimental
Arm Description
A distal regional anaesthesia is performed in which the nerves are blocked by a local anaesthetic in the tissue in the immediate vicinity of the operating area ("tissue infiltration technique"). The LIA is applied in a total of 4 steps during the preparation of the knee joint: 1. after the skin incision, 2. after the capsule incision, 3. after complete exposure of the knee joint, 4. when the posterior knee capsule is reached.
Arm Title
Late-intraoperative Local infiltration technique
Arm Type
Active Comparator
Arm Description
A distal regional anaesthesia is performed in which the nerves are blocked by a local anaesthetic in the tissue in the immediate vicinity of the operating area ("tissue infiltration technique"). The LIA is applied after the preparation of the femur and tibia bone shortly before the prosthesis is inserted and during the retreat from the knee joint.
Intervention Type
Procedure
Intervention Name(s)
Late local infiltration analgesia
Other Intervention Name(s)
late LIA
Intervention Description
Patient receive an infiltration of local anaesthetics around the knee directly after total knee replacement for postoperative pain control.
Intervention Type
Procedure
Intervention Name(s)
Early local infiltration analgesia
Other Intervention Name(s)
early LIA
Intervention Description
The local infiltration analgesia is applied in a total of 4 steps during the preparation of the knee joint: 1. after the skin incision, 2. after the capsule incision, 3. after complete exposure of the knee joint, 4. when the posterior knee capsule is reached.
Primary Outcome Measure Information:
Title
Opioid consumption
Description
amount of opioids administered intraoperative measured as equivalent dose to morphin
Time Frame
intraoperative, up to 3 hours
Secondary Outcome Measure Information:
Title
time to first mobilisation (standing)
Description
time from end of surgery until patients is able to stand
Time Frame
up to 48 hours postoperatively
Title
patients satisfaction (11-point likert scale)
Description
global satisfaction of patients
Time Frame
up to 7 days postoperatively
Title
time to first mobilisation (walking)
Description
time from end of surgery until patients is able to walk
Time Frame
up to 7 days postoperatively
Title
time to achieve full joint mobility
Description
time to achieve full joint mobility (0/0/90°)
Time Frame
up to 7 days postoperatively
Title
Janda grade of both legs at first day after surgery
Description
best Janda grade in both legs the day after surgery
Time Frame
up to 24h postoperatively
Title
Pain intensity
Description
intensity of pain in all patients meausered by numeric rating scale (NRS)
Time Frame
up to 7 days postoperatively
Title
rescue pain medication
Description
number of patients requiring rescue pain medication
Time Frame
up to 7 days postoperatively
Title
time to discharge
Description
time to discharge from hospital
Time Frame
up to 14 days postoperatively
Title
Opioid consumption (hospital)
Description
amount of opioids administered until discharge measured as equivalent dose to morphin
Time Frame
up to 14 days postoperatively
Title
delirium
Description
incidence of postoperative delirium measured by Nursing Delirium Screening Scale (NuDeSc)
Time Frame
up to 7 days postoperatively
Title
postoperative nausea and vomiting (PONV)
Description
incidence of PONV
Time Frame
up to 7 days postoperatively
Title
surgeon satisfaction (6-point likert scale)
Description
satisfaction of surgeon in points of clarity of the operative field, change of the operative field by LIA and overall satisfaction represented in one value
Time Frame
intraoperative, up to 3 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • patients undergoing elective, primary knee joint replacement in combined general anaesthesia Exclusion Criteria: heart insufficiency NYHA >2 liver insufficiency > CHILD B evidence of diabetic polyneuropathy severe adipositas BMI >40 patients < 18 years pregnancy in case of police custody participation in a paralleled interventional RCT in a time frame of 30 days chronic opioid therapy >3 months before scheduled surgery allergy against medication required for surgery or anaesthesia
Facility Information:
Facility Name
Charité - Universitätsmedizin Berlin
City
Berlin
ZIP/Postal Code
10117
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
21312140
Citation
Morin AM, Wulf H. [High volume local infiltration analgesia (LIA) for total hip and knee arthroplasty: a brief review of the current status]. Anasthesiol Intensivmed Notfallmed Schmerzther. 2011 Feb;46(2):84-6. doi: 10.1055/s-0031-1272875. Epub 2011 Feb 10. German.
Results Reference
background
PubMed Identifier
26227482
Citation
Perret M, Fletcher P, Firth L, Yates P. Comparison of patient outcomes in periarticular and intraarticular local anaesthetic infiltration techniques in total knee arthroplasty. J Orthop Surg Res. 2015 Jul 31;10:119. doi: 10.1186/s13018-015-0249-x.
Results Reference
background
PubMed Identifier
16950075
Citation
Peters CL, Shirley B, Erickson J. The effect of a new multimodal perioperative anesthetic regimen on postoperative pain, side effects, rehabilitation, and length of hospital stay after total joint arthroplasty. J Arthroplasty. 2006 Sep;21(6 Suppl 2):132-8. doi: 10.1016/j.arth.2006.04.017.
Results Reference
background
PubMed Identifier
26321550
Citation
Suthersan M, Pit S, Gordon L, Loman M, Pezzutti B, Freihaut R. Local infiltration analgesia versus standard analgesia in total knee arthroplasty. J Orthop Surg (Hong Kong). 2015 Aug;23(2):198-201. doi: 10.1177/230949901502300217.
Results Reference
background
PubMed Identifier
30562225
Citation
Kastelik J, Fuchs M, Kramer M, Trauzeddel RF, Ertmer M, von Roth P, Perka C, Kirschbaum SM, Tafelski S, Treskatsch S. Local infiltration anaesthesia versus sciatic nerve and adductor canal block for fast-track knee arthroplasty: A randomised controlled clinical trial. Eur J Anaesthesiol. 2019 Apr;36(4):255-263. doi: 10.1097/EJA.0000000000000929.
Results Reference
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Optimization of a Fast-track Concept for Knee Joint Replacement

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