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Clinical Trial Summary

The ActiPatch is a cutaneous device which is CE marked approved for relief of pain. It is taped over the affected area and stimulation at a high frequency is reported to alleviate pain with no sensation. However there is no class 1 evidence for this on back pain. By randomising patients between application of an active device or a dummy device and assessment of disability and pain scores at two weeks, the efficacy or otherwise can be established. Low back pain is a major health problem and if effective this has major economic implications as the device is cheap and safe.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02601807
Study type Interventional
Source University of Oxford
Contact Tipu Z Aziz
Phone 01865231885
Email tipu.aziz@nds.ox.ac.uk
Status Recruiting
Phase N/A
Start date August 2015

See also
  Status Clinical Trial Phase
Completed NCT03106740 - Evaluating the Role of Neuroinflammation in Low Back Pain Phase 2