Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients

PHASE4CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

January 31, 2010

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
Diabetes Mellitus
Interventions
DRUG

Basal-bolus detemir-aspart insulin regimen

After the first CGM was completed during the conventional anti-diabetic treatment, patients received a rapid-acting insulin analogue before each meal (i.e., aspart) and a basal long-acting insulin analogue (i.e., detemir) once or twice daily. The analogues were titrated for optimal glycemic control. After one month of the aspart and detemir regimen, a physician adapted the insulin doses according to the glucose values observed from the second CGM.

Trial Locations (5)

59300

Regional Hospital of Valenciennes, Valenciennes

67000

Sainte Anne Hospital, Strasbourg

University Hospital of Strasbourg, Strasbourg

68000

Regional Hospital of Colmar, Colmar

68100

Regional Hospital of Mulhouse, Mulhouse

Sponsors

Collaborators (2)

All Listed Sponsors
collaborator

Novo Nordisk A/S

INDUSTRY

collaborator

Abbott

INDUSTRY

lead

Centre Europeen d'Etude du Diabete

OTHER