Wound Study

How will the study be conducted?

  1. Participants will be given non-invasive, hand-held, battery operated, microcurrent device kits to use during the study. The kit consists of the Tennant Biomodulator® Plus, pads and lead wires. After you complete the study, the device will be yours to keep to continue your wound healing process.

  2. The microcurrent stimulation, using the devices, will be used as additional treatment to participants current standard of care treatment.

  3. The study will last approximately 4 weeks with one follow up visit 30 days after the participant’s final treatment visit.

  4. Participants are required to schedule weekly visits for the duration of the study. These visits can be combined with the existing appointments. The remainder of the daily treatments can be done at home.

What is microcurrent stimulation?
Microcurrent stimulation uses electrical energy that passes into the tissue, stimulating internal electrical and chemical processes around the chronic wound tissue. The treatment is thought to be effective in improving circulation, accelerating tissue regeneration and reducing inflammation.

The Potential Benefits to Participants Are:

  • Narcotic-Free Pain Relief
    The devices are FDA cleared for pain management.

  • Wound Healing
    The devices use electrical energy that passes into tissue, stimulating internal electrical and chemical processes. The treatment might be effective in improving circulation, accelerating tissue regeneration and reducing inflammation.

  • Mobility
    Some patients find that chronic wound pain makes daily tasks difficult. The device might cause reduction in pain and wound size so that some patients might be able to resume their daily activities.

 

Click here to download Wound Study Qualifying Application
Click here to download Complete Wound Study Brochure

 




 
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