HHC Lymphflow Go PCD evaluation
Research type
Research Study
Full title
A Pilot evaluation on the Use of the Haddenham (HHC) Lymphflow Go Pneumatic Compression Device (PCD) in Oedema related to Lymphoedema and Chronic Venous Insufficiency.
IRAS ID
355616
Contact name
Natalie Phillips
Contact email
Sponsor organisation
Haddenham Healthcare
Duration of Study in the UK
0 years, 3 months, 0 days
Research summary
A portable pneumatic compression device is a new concept in lymphoedema and Chronic Venous Insufficiency (CVI). The current predecessor devices are bulky, not portable and not clear in their instructions for use. This new device has been developed to address these challenges with portability and ease of use whilst encompassing two treatment modes with 3 different pressure profiles. The literature details conflicting information on levels of pressure or modes of treatment with no clear consensus to guide treatment choices.
This small pilot study aims to demonstrate safety and efficacy of the product in a small cohort of patients, with emphasis placed on the portability and usability of the device and whether the device is a useful adjunct to self-care which in turn will reduce the burden of self-management on the patient as visits to the clinical settings can be reduced. Furthermore, research has shown a reduction in infections associated with lymphoedema, which in turn reduces the burden on the health service.REC name
North of Scotland Research Ethics Committee 1
REC reference
25/NS/0042
Date of REC Opinion
14 May 2025
REC opinion
Further Information Favourable Opinion