Auricular Acupuncture for Pain Relief After Ambulatory Knee Arthroscopy

This study has been completed.
Sponsor:
Information provided by:
University Medicine Greifswald
ClinicalTrials.gov Identifier:
NCT00233857
First received: October 5, 2005
Last updated: February 25, 2011
Last verified: February 2011

October 5, 2005
February 25, 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 ClinicalTrials.gov 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
Not Provided
Not Provided
 
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

Not Provided
Interventional
Phase 2
Phase 3
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Postoperative Pain
Procedure: Auricular acupuncture
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
120
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.
Both
16 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT00233857
III UV 23/03
Not Provided
Not Provided
University Medicine Greifswald
Not Provided
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