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PEMF Effects on Pain After Abdominal Body Contouring

Sponsor
University of Pittsburgh (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01762423
Collaborator
(none)
0
Enrollment
1
Location
2
Arms
2
Duration (Months)
0
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Body contouring surgery has a higher potential for postoperative pain and wound healing complications. The purpose of this study is to determine if pulsed electromagnetic field (PEMF) devices can reduce the pain and complications associated with this type of surgery.

Pulsed electromagnetic field (PEMF) devices have been shown to be effective treatments to decrease healing time in nonunion fractures and pressure ulcers, and to reduce pain in whiplash injuries, persistent neck pain, and chronic lower back pain. These devices have been FDA approved for treatment of pain and edema (510(k) number: K070541). More recently, PEMF devices have been shown to decrease postoperative pain and narcotic use in breast augmentation patients. This study seeks to determine if PEMF will also cause similar effects in the more complex procedures performed on body contouring patients. The specific aims of this study are:

  1. Evaluate if adjunct PEMF therapy will accelerate the rate of postoperative pain reduction in abdominal body contouring patients.

  2. Evaluate if adjunct PEMF therapy will decrease the postoperative use of narcotic pain relievers in abdominal body contouring patients.

PEMF devices have been shown to be effective in reduction of pain and pain medication use in breast augmentation patients. No literature has shown if PEMF is an effective adjunct to decrease pain or pain medication use in the abdominal body contouring patient. A decrease in pain would result in a better experience for patients and a reduction in pain medication may decrease complications associated with these medications. The PEMF therapy device being used in this study is a non-significant risk device because it is noninvasive and does not present a potential for serious risk to the health, safety, or welfare of a subject.

Condition or Disease Intervention/Treatment Phase
  • Device: Active Device (IVIVI SofPulse)
  • Device: Sham Device
 Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
PEMF Effects on Pain After Abdominal Body Contouring
Study Start Date :
Dec 1, 2012
Actual Primary Completion Date :
Feb 1, 2013
Actual Study Completion Date :
Feb 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Active Device

Device Placement: Upon completion of the subjects' standard of care body contouring surgery, the device will be placed directly on the operative dressings within an unobtrusive binder with Velcro strips and will be activated before the subject leaves the OR. Subjects will then be educated on the functionality and interpretation of the user interface of the device. They will be educated on the application, removal, and return of the device. Active Devices The device will be activated at the time of placement. The active devices are programmed to automatically deliver treatment. Each treatment duration is 15 minutes. The active device delivers treatment every 2 hours. A light will flash on the device when the PEMF begins and will continue to flash every second until the end of the treatment. Between treatments the device will be in "sleep mode" and the light will flash every 5 seconds.

Device: Active Device (IVIVI SofPulse)
Other Names:
  • IVIVI SofPulse

    		•
    Sham Comparator: Sham Device

    Device Placement: Upon completion of the subjects' standard of care body contouring surgery, the device will be placed directly on the operative dressings within an unobtrusive binder with velcro strips and will be activated before the subject leaves the OR. Subjects will then be educated on the functionality and interpretation of the user interface of the device. They will be educated on the application, removal, and return of the device. Sham Devices The sham devices mirror the active device with the exception of the delivery of the PEMF. The sham device will be "activated" at the time of placement. A light will flash on the device when the SHAM PEMF begins and will continue to flash every second until the end each treatment interval. While in "sleep mode" the device will not deliver treatment and the light will flash every 5 seconds.

    Device: Sham Device

    Outcome Measures

    Primary Outcome Measures

    1. Postoperative Pain Reduction [Immediately postoperatively through 6 days postoperative]

      Evaluate if adjunct PEMF therapy will accelerate the rate of postoperative pain reduction in abdominal body contouring patients.

    Secondary Outcome Measures

    1. Postoperative Narcotic Use [Immediately postoperative through 6 day postoperative]

      Evaluate if adjunct PEMF therapy will decrease the postoperative use of narcotic pain relievers in abdominal body contouring patients.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • Age: 18 years and older and able to provide informed consent

    • Eligible for and have agreed to be scheduled for elective abdominal body contouring surgery

    • Willing and able to comply with all study procedures.

    Exclusion Criteria:

    • Inability to provide informed consent

    • Patients having multiple procedures concurrently except liposuction.

    • Current use of oral steroids as determined through patient history and medical record review

    • Current narcotic use as determined through patient history or medical record review

    • Current nerve or pain disorder.

    • Recent (1 month) coronary stent or implanted medical device (e.g. pacemaker).

    • Pregnancy (demonstrated by a positive result of a urine pregnancy test)

    • Based upon surgeon judgement and the results of screening procedures, patient is not a suitable candidate for surgery.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UPMC Center for Innovation in Restorative Medicine Pittsburgh Pennsylvania United States 15213

    Sponsors and Collaborators

    • University of Pittsburgh

    Investigators

    • Principal Investigator: J. Peter Rubin, MD, University of Pittsburgh

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    J. Peter Rubin, MD, Principal Investigator, University of Pittsburgh
    ClinicalTrials.gov Identifier:
    NCT01762423
    Other Study ID Numbers:
    • PRO12070504
    First Posted:
    Jan 7, 2013
    Last Update Posted:
    Feb 20, 2013
    Last Verified:
    Feb 1, 2013
    Additional relevant MeSH terms:
    Pain, Postoperative

    Study Results

    No Results Posted as of Feb 20, 2013