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Efficiency Study About the Effect of Acupuncture on Postoperative Pain After Total Knee Arthroplasty (APOPKA)

Primary Purpose

Pain, Postoperative

Status
Unknown status
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
acupuncture/PCA/NSAID
sham acupuncture/PCA/NSAID
PCA/NSAID
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain, Postoperative

Eligibility Criteria

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

Inclusion Criteria:

  • patients with advanced osteoarthritis of the knee (primary and secondary reasons)
  • planned surgical procedure TKA

Exclusion Criteria:

  • renal insufficiency
  • cardial insufficiency
  • coronary heart disease
  • regular therapeutic use of morphines, hydrocodones, benzodiazepines before surgery.

Sites / Locations

  • Vienna General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Sham Comparator

Other

Arm Label

acupuncture/PCA/NSAID

sham acupuncture/PCA/NSAID

PCA/NSAID

Arm Description

standard program with defined points: Ear acupuncture needles bitten once (day 0-5) Body acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5 - 1 cm, with DeQI feeling/sensation is released

standard program with defined points: Ear sham-acupuncture needles bitten once (day 0-5) Body sham-acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5

minimal intervention (included in every arm) standard boli of morphine by pressing a button of PCA availability in the postoperative period (day 0-4) readout once a day NSAID (non-steroid antiinflammatory drug) 2x i.v. (75mg diclofenac-sodium, 30 mg orphenadrine citrate) (day 0-4)

Outcomes

Primary Outcome Measures

Amount of morphines/day
Morphine PCRA (pain pump) administered to every patient

Secondary Outcome Measures

movement abilities
range of motion/Knee society score
Quality of Life (QOL)
SF36 (short form 36)
Pain intensity (VAS)

Full Information

First Posted
May 25, 2015
Last Updated
May 27, 2015
Sponsor
Medical University of Vienna
Collaborators
Medical Scientific Fund of the Mayor of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT02456116
Brief Title
Efficiency Study About the Effect of Acupuncture on Postoperative Pain After Total Knee Arthroplasty
Acronym
APOPKA
Official Title
Efficiency Study About the Effect of Acupunctur on Postoperative Pain After Total Knee Arthroplastry
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2012 (undefined)
Primary Completion Date
September 2015 (Anticipated)
Study Completion Date
September 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna
Collaborators
Medical Scientific Fund of the Mayor of Vienna

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the use of needle acupuncture in comparison to a conventional postoperative pain management in terms of reducing pain and pain medication use in an interdisciplinary setting in a controlled, randomized study design after implantation of total knee arthroplasty .
Detailed Description
Patients and Methods 1.1 All patients will be treated at the Medical University of Vienna and receive a TKA due to advanced gonarthrosis. The study includes male and female patients. Every patient who is admitted for a TKA ( Total knee arthroplasty) implant is invited to take part in the study. Exclusion criteria: renal insufficiency, cardial insufficiency, coronary heart disease, use of morphines, hydrocodones, benzodiazepines before surgery. 1.2 The acupuncture is carried out using sterile disposable acupuncture needles, steel with a copper coil, size 0.25 x 30 mm by experienced acupuncturists and students in their third training year of the post graduate TCM (traditionel chinese medicine) training course of the Medical University of Vienna. The standard acupuncture was compiled as a traditional Chinese conventional body and ear/auricular acupuncture by a consortium of acupuncture professors as follows: Body acupuncture, pricked from both sides, the depth of the prick 0.5 - 1 cm, according to the technique of traditional Chinese acupuncture a DeQI (a sensation in the area of the acupuncture or in the course of the corresponding meridian) released. Regarding the frequency: ear acupuncture needles are bitten only postoperatively and can be left for a period of 4 until 7 postoperative days . The body acupuncture needling is carried out at the points of question once a day for a period of about 20 minutes , starting at the first preoperative day, continuating the day of surgery and 2nd and 4th postoperative day. In sham acupuncture the given acupuncture points are pricked 2-3 centimetres from the defined point. The group of patients who is not receiving any acupuncture and only used the PCA (Patient Controlled Analgesia) pain pump therapy is chosen as a control group. The pain pump therapy is not the subject of this clinical study and is routinely used for postoperative pain in TKA operations and does not need any evaluation. 1.3 Randomising Patients who agree to take part in the study are randomised and blinded for the surgeon into 3 groups regarding the planned pain therapy. For postoperative pain therapy all patients receive, an on demand pain pump with morphine with controlled amounts of analgesics. The groups were formed on the assumption of a 30% reduction of pain using acupuncture in a power analysis with α=…… assuming 3 groups with 30 people each.: The method of randomising occurs as a sequence. The blinding applied especially to the surgeon and the patients who received real and sham acupuncture. Outcome measures: The primary aim is to find out if additive pain therapy in the form of body and ear/auricular acupuncture can effectively prove pain reduction after TKA implantation. The amount of applied analgesics on every postoperative day (1.-5.) defines the command variable. The efficiency of acupuncture should be measured accordingly to the reduction of the on demand pain pump therapy. Secondary objectives are the VAS of every postoperative day (1.-5.), the assessment of the operated leg's mobility as well as peri-operative nausea. The intensity of pain is recorded as follows: A) indirectly using the protocol of the amount of morphine administered by the PCA pump B) measuring pain by VAS (routinely 3 x daily)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
acupuncture/PCA/NSAID
Arm Type
Experimental
Arm Description
standard program with defined points: Ear acupuncture needles bitten once (day 0-5) Body acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5 - 1 cm, with DeQI feeling/sensation is released
Arm Title
sham acupuncture/PCA/NSAID
Arm Type
Sham Comparator
Arm Description
standard program with defined points: Ear sham-acupuncture needles bitten once (day 0-5) Body sham-acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5
Arm Title
PCA/NSAID
Arm Type
Other
Arm Description
minimal intervention (included in every arm) standard boli of morphine by pressing a button of PCA availability in the postoperative period (day 0-4) readout once a day NSAID (non-steroid antiinflammatory drug) 2x i.v. (75mg diclofenac-sodium, 30 mg orphenadrine citrate) (day 0-4)
Intervention Type
Device
Intervention Name(s)
acupuncture/PCA/NSAID
Intervention Description
standard program with defined points: Ear acupuncture needles bitten once (day 0-5) Body acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5 - 1 cm, with DeQI feeling/sensation is released
Intervention Type
Device
Intervention Name(s)
sham acupuncture/PCA/NSAID
Intervention Description
standard program with defined points: Ear acupuncture needles bitten once (day 0-5) Body acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5
Intervention Type
Other
Intervention Name(s)
PCA/NSAID
Intervention Description
standard boli of morphine by pressing a button of PCA
Primary Outcome Measure Information:
Title
Amount of morphines/day
Description
Morphine PCRA (pain pump) administered to every patient
Time Frame
1.-4.day postoperative
Secondary Outcome Measure Information:
Title
movement abilities
Description
range of motion/Knee society score
Time Frame
1.-4.day postoperative
Title
Quality of Life (QOL)
Description
SF36 (short form 36)
Time Frame
day -1/day 5
Title
Pain intensity (VAS)
Time Frame
1.-4.day postoperative

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with advanced osteoarthritis of the knee (primary and secondary reasons) planned surgical procedure TKA Exclusion Criteria: renal insufficiency cardial insufficiency coronary heart disease regular therapeutic use of morphines, hydrocodones, benzodiazepines before surgery.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Reinhard Windhager, Prof. Dr.
Phone
+4314040040820
Email
reinhard.windhager@akhwien.at
First Name & Middle Initial & Last Name or Official Title & Degree
Bernd Kubista, Prof. Dr.
Phone
+4314040040830
Email
bernd.kubista@meduniwien.ac.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerhard M Hobusch, Dr.
Organizational Affiliation
Medical University of Vienna, Department of Orthopaedics
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vienna General Hospital
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerhard M Hobusch, Dr.
Phone
+4314040040830
Email
gerhard.hobusch@meduniwien.ac.at
First Name & Middle Initial & Last Name & Degree
Bernd Kubista, Prof. Dr.
Phone
+4314040040830
Email
bernd.kubista@meduniwien.ac.at

12. IPD Sharing Statement

Citations:
PubMed Identifier
19222107
Citation
Lin JG, Chen WL. Review: acupuncture analgesia in clinical trials. Am J Chin Med. 2009;37(1):1-18. doi: 10.1142/S0192415X09006679.
Results Reference
background
PubMed Identifier
22712373
Citation
Wang JF, Bao HX, Cai YH, Zhang JH, Tong PJ. [Case-control study on application of auricular acupuncture for the treatment of analgesia during perioperative period in total hip arthroplasty]. Zhongguo Gu Shang. 2012 Mar;25(3):220-3. Chinese.
Results Reference
background
PubMed Identifier
17224599
Citation
Usichenko TI, Kuchling S, Witstruck T, Pavlovic D, Zach M, Hofer A, Merk H, Lehmann C, Wendt M. Auricular acupuncture for pain relief after ambulatory knee surgery: a randomized trial. CMAJ. 2007 Jan 16;176(2):179-83. doi: 10.1503/cmaj.060875.
Results Reference
background

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Efficiency Study About the Effect of Acupuncture on Postoperative Pain After Total Knee Arthroplasty

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