Guidance
Evidence-based recommendations on electrical stimulation of the lower oesophageal sphincter for treating gastro-oesophageal reflux disease.
The EndoStim device used for this procedure is no longer available and there are currently no other CE-marked devices available. A non CE-marked device can only be used in the context of clinical trials, with MHRA and research ethical approval. See MHRA advice on off-label use of a medical device.
Guidance development process
How we develop NICE interventional procedures guidance
Coding and clinical classification codes for this guidance