About this trial

This study is designed to evaluate the efficacy and safety of endoscopic duodenal re-cellularization therapy using pulsed electric field in individuals with in patients with a recent diagnosis of type 2 diabetes mellitus (T2DM).

Eligibility criteria

Qualifiers

Duration of T2DM </= 2 years

HbA1c </= 7.5%

On 0-1 oral diabetes medications

Disqualifiers

Previous treatment with pulsENDO or similar procedure

Previous GI surgery that could preclude the ability to perform pulsENDO, or acute gastric and duodenal pathology that increased the risk of pulsENDO

Type I DM, DM secondary to specific disease or having any history of ketoacidosis

Fasting C-peptide level <0.5ug/L

Trial design

Treatments tested in this trial

  • pulsENDO treatment

Treatment groups

40 Participants
are divided into 1 treatment group

Locations

1
Chinese University of Hong Kong Shatin Hong Kong

Sponsors and collaborators

Chinese University of Hong Kong

Lead sponsor