The Set-Point Study: Evaluating Effects of Changing Glucose Target on Bionic Pancreas Performance

NACompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

August 31, 2015

Primary Completion Date

December 31, 2017

Study Completion Date

December 31, 2017

Conditions
Type 1 DiabetesType 2 Diabetes
Interventions
DEVICE

Bionic Pancreas

Participant wears the bionic pancreas, including an insulin and/or glucagon pump depending on which arm they are in. The 100 mg/dl arm for type 1 diabetes patients will deliver insulin and glucagon. The 100 mg/dl arm for type 2 diabetes patients will deliver just insulin. The 115 mg/dl arm will deliver insulin and glucagon. The 120 mg/dl arm will deliver just insulin. The 145 mg/dl arm will deliver just insulin. The 130 mg/dl and 110 mg/dl arms will deliver insulin and placebo, or insulin and glucagon, and will be double blinded.

OTHER

Usual Care

Participant cares for their diabetes according to their usual practice, with blinded CGM monitoring. No medication will be administered by the study in this intervention.

Trial Locations (1)

02114

Masscahusetts General Hospital, Boston

All Listed Sponsors
lead

Massachusetts General Hospital

OTHER

NCT02509065 - The Set-Point Study: Evaluating Effects of Changing Glucose Target on Bionic Pancreas Performance | Biotech Hunter | Biotech Hunter