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Pain, PostoperativeAPOPKANCT02456116

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

A study testing acupuncture/PCA/NSAID and PCA/NSAID in people with Pain, Postoperative, run by Medical University of Vienna at 1 site in Austria.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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 . Read more about this study

Who is it for?
Any age
Conditions the study is for
Pain, Postoperative
What is being tested?
acupuncture/PCA/NSAID and PCA/NSAID
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
90 participants
Where
1 siteAustria
Study dates
Sep 2012to Sep 2015
Phase
Interventional
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 Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Reinhard Windhager, Prof. Dr. contact

+4314040040820

reinhard.windhager@akhwien.at

Bernd Kubista, Prof. Dr. contact

+4314040040830

bernd.kubista@meduniwien.ac.at

Austria1 site, 1 recruiting
  • Vienna General Hospital

    Vienna, 1090

    Gerhard M Hobusch, Dr., +4314040040830, gerhard.hobusch@meduniwien.ac.at

    Bernd Kubista, Prof. Dr., +4314040040830, bernd.kubista@meduniwien.ac.at

    Recruiting

Other trials in Austria

About this study

Official title: Efficiency Study About the Effect of Acupunctur on Postoperative Pain After Total Knee Arthroplastry

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 .

Read the detailed description
  1. 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.
  2. 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:

  1. indirectly using the protocol of the amount of morphine administered by the PCA pump B) measuring pain by VAS (routinely 3 x daily)
Being tested
acupuncture/PCA/NSAID, sham acupuncture/PCA/NSAID, PCA/NSAID
Medical subject headings
Pain, Postoperative

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • acupuncture/PCA/NSAIDDevice

    standard program with defined points:

    1. Ear acupuncture needles bitten once (day 0-5)
    2. 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
  • sham acupuncture/PCA/NSAIDDevice

    standard program with defined points:

    1. Ear acupuncture needles bitten once (day 0-5)
    2. Body acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5
  • PCA/NSAIDOther

    standard boli of morphine by pressing a button of PCA

Study groups in NCT02456116
Study groupRoleWhat they receive
acupuncture/PCA/NSAIDExperimentalstandard program with defined points: 1. Ear acupuncture needles bitten once (day 0-5) 2. 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
Receives: Device: acupuncture/PCA/NSAID
sham acupuncture/PCA/NSAIDSham comparatorstandard program with defined points: 1. Ear sham-acupuncture needles bitten once (day 0-5) 2. Body sham-acupuncture, once a day 20 minutes (day -1/ 0/ 2/ 4), depth of the prick 0.5
Receives: Device: sham acupuncture/PCA/NSAID
PCA/NSAIDOtherminimal 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)
Receives: Other: PCA/NSAID

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Amount of morphines/day

    Morphine PCRA (pain pump) administered to every patient

    Measured: 1.-4.day postoperative

Secondary outcomes (3)
  1. movement abilities

    range of motion/Knee society score

    Measured: 1.-4.day postoperative

  2. Quality of Life (QOL)

    SF36 (short form 36)

    Measured: day -1/day 5

  3. Pain intensity (VAS)

    Measured: 1.-4.day postoperative

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 May 2015 (estimated)
  2. Study startSep 2012
  3. Primary completionSep 2015 (estimated)
  4. Study completionSep 2015 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02456116
Sponsor's protocol ID
KP13067BGMPOA
Acronym
APOPKA
Status last verified
May 2015
First submitted
25 May 2015
Last updated
28 May 2015
Results posted
No
Data monitoring committee
No

Publications

  • Lin JG, Chen WL. Review: acupuncture analgesia in clinical trials. Am J Chin Med. 2009;37(1):1-18. doi: 10.1142/S0192415X09006679.

    PubMed 19222107
  • 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.

    PubMed 22712373
  • 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.

    PubMed 17224599

Questions about this trial

What is this clinical trial studying?

A study testing acupuncture/PCA/NSAID and PCA/NSAID in people with Pain, Postoperative, run by Medical University of Vienna at 1 site in Austria.

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 2 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 28 May 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. 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?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Reinhard Windhager, Prof. Dr. (+4314040040820, reinhard.windhager@akhwien.at), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Amount of morphines/day (time frame: 1.-4.day postoperative). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02456116, which also lists 3 linked publications.

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 28 May 2015.

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