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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00455182
Date of registration: 29/03/2007
Primary sponsor: HealthEast Care System
Public title: Acupuncture for Pain Management After Hip or Knee Arthroplasty
Scientific title: Acupuncture for Pain Management After Hip or Knee Arthroplasty
Date of first enrolment: March 2007
Target sample size: 90
Recruitment status: Withdrawn
URL:  http://clinicaltrials.gov/show/NCT00455182
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment  
Countries of recruitment
United States
Contacts
Name:   Daniel Hoeffel, M.D.
Address: 
Telephone:
Email:
Affiliation:  Summit Orthopedics
Key inclusion & exclusion criteria

Inclusion Criteria:

- 18-80 years old

- Undergoing total hip or total knee arthroplasty

- Spinal anesthesia during surgery

Exclusion Criteria:

- Arthroplasty of contralateral limb within the past three months

- Medical condition, in judgement of examiner, that may preclude safe participation
in protocol or prevents completion of the study

- General anesthesia

- Use of any investigational drug in the past 30 days

- Has received acupuncture in the past

- Currently participating in another interventional study

- Unwilling to be randomized

- Patients who request Healing Touch, another form of alternative treatment that is
offered at Woodwinds Hospital.



Age minimum: 18 Years
Age maximum: 80 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Pain
Postoperative Complications
Intervention(s)
Procedure: Acupuncture
Procedure: Sham Acupuncture
Procedure: Standard medical care
Primary Outcome(s)
Pain intensity as measured by the Visual Analog Scale [Time Frame: Before and immediately following treatment]
Pain medication use [Time Frame: before and after treatment]
Secondary Outcome(s)
Cost of pain treatment [Time Frame: Annually]
Secondary ID(s)
HE 06 10 007
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Northwestern Health Sciences University
University of Minnesota - Clinical and Translational Science Institute
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