Auricular Acupuncture for Pain Relief After Ambulatory Knee Arthroscopy

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. Identifier: NCT00233857
Recruitment Status : Completed
First Posted : October 6, 2005
Last Update Posted : February 28, 2011
Information provided by:
University Medicine Greifswald

October 5, 2005
October 6, 2005
February 28, 2011
August 2003
July 2004   (Final data collection date for primary outcome measure)
Postoperative ibuprofen requirement after the surgery
Same as current
Complete list of historical versions of study NCT00233857 on Archive Site
Pain intensity assessed by patients on VAS-100 ; total piritramide requirement in anesthesia recovery room; incidence of analgesia-related side effects
Same as current
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Auricular Acupuncture for Pain Relief After Ambulatory Knee Arthroscopy
Auricular Acupuncture Versus Placebo (Sham Acupuncture) for Postoperative Pain Relief After Ambulatory Knee Arthroscopy - a Randomized Controlled Trial
The aim was to investigate whether auricular acupuncture is superior to sham acupuncture in relief of acute postoperative pain and in reduction of analgesics consumption on demand and their side effects in patients after ambulatory knee arthroscopy
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Phase 2
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Postoperative Pain
Procedure: Auricular acupuncture
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*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Same as current
August 2004
July 2004   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Patients with an American Society of Anesthesiologists physical status of I to II scheduled for ambulatory knee arthroscopy under general anesthesia.
  2. Surgery time does not exceed 60 minutes.
  3. Patients without previous opioid and/or psychiatric medication.
  4. Patients ranged 16-65 years old.
  5. Patients able to use Visual Analogue Scale-100 for pain intensity measurement.
  6. Patients who have given informed consent.

Exclusion Criteria:

  1. Pregnant or nursing females.
  2. Recidivist alcoholics and/or patients with history of psychiatric disease.
  3. Local or systemic infection.
  4. Age < 16 and > 65 years.
  5. Surgery time more than 60 minutes.
  6. Inability to use Visual Analogue Scale-100.
  7. Patients consumed opioid medication before surgery.
  8. Patients with prosthetic or damaged cardiac valves (s. Potential risks)
  9. Patients who are unable to understand the consent form.
Sexes Eligible for Study: All
16 Years to 65 Years   (Child, Adult, Older Adult)
Contact information is only displayed when the study is recruiting subjects
III UV 23/03
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University Medicine Greifswald
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Principal Investigator: Taras I. Usichenko, Assistant Professor Anesthesiology and Intensive Care Medicine Department, Ernst Moritz Arndt University of Greifswald, Germany
University Medicine Greifswald
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP