Type 2 Diabetes Mellitus Clinical Trial
Official title:
Study of Sulphonylurea Synergy With Incretins
The Study of Sulphonylurea Synergy with Incretins (LOGIC) is a Proof-of-Concept Physiological
study in the form of two matched isoglycaemic clamps. A matched clamp consists of an of oral
glucose tolerance test followed by an isoglycaemic intravenous glucose infusion (IGII). The
study will investigate whether there is synergy between a physiological sulphonylurea (SU)
stimulus and the incretin effect, causing augmentation of insulin secretion in patients with
type 2 diabetes mellitus (T2DM). The study will take place at The Clinical Research Centre at
Ninewells Hospital in Dundee over five visits. It will evaluate 20 patients with T2DM on no
diabetes therapy, or metformin monotherapy.
All participants will undergo two matched clamps. The first matched clamp will be with no
intervention. The second intervention matched clamp, low-dose liquid gliclazide will be
administered 1-hour prior to each test. The sulphonylurea, Gliclazide, in this this instance
will be used as a physiological stimulus and will only be given on two occasions as part of
the second matched clamp. The first eight participants will participate in the dose-ranging
phase. They will receive either 10mg or 20mg gliclazide as a stimulus to augment the incretin
effect. A further twelve participants will then be recruited to complete the study utilising
the dose which caused the greatest increment in insulin secretion. LOGIC will also evaluate
the cohort for effect of KCNJ11 genotype on physiological response.
The Study of Sulphonylurea Synergy with Incretins (LOGIC) is a Proof-of-Concept Physiological
study in the form of two matched isoglycaemic clamps. A matched clamp consists of an of oral
glucose bolus test followed by an isoglycaemic intravenous glucose infusion (IGII) the next
day. The study will investigate whether there is synergy between a physiological
sulphonylurea (SU) stimulus and the incretin effect, causing augmentation of insulin
secretion in patients with type 2 diabetes mellitus (T2DM).
The study will take place at The Clinical Research Centre at Ninewells Hospital in Dundee
over five visits. It will evaluate 20 patients with T2DM on no diabetes therapy, or metformin
monotherapy.
The first visit is a screening visit to ensure the participant meets inclusion and exclusion
criteria, and, if so, to obtain written informed consent for study. Visits 2-5 will all occur
following an overnight 10-hour fast at home. The second and third visits will make up the
first matched clamp. In visit 2, the participant will undergo a 75-gram oral glucose bolus
with frequent blood sampling to assess the glucose variance, insulin secretion and incretin
hormone response from an oral glucose stimulus. Blood glucose level (BGL) will be sampled
every 5 minutes along with hormone biochemical analysis at regular defined time points. The
third visit consists of an IGII to replicate the glucose curve from the OGTT to allow
measurement of incretin effect. BGL will again be sampled every 5 minutes with regular
biochemical analysis of hormones.
The investigators aim to establish whether a low-dose of sulphonylurea will have a
synergistic role on insulin secretion with endogenously secreted GLP-1 and GIP, therefore
visits four and five will complete the same matched clamp, however, low-dose liquid
gliclazide will be administered 1-hour prior to each test. The sulphonylurea, Gliclazide, in
this this instance will be used as a physiological stimulus and will only be given on two
occasions as part of the second matched clamp. The first eight participants will receive
either 10mg or 20mg gliclazide as a stimulus to augment the incretin effect. A further twelve
patients will then be recruited to complete the study utilising the dose which caused the
greatest increment in insulin secretion.
The comparison of these tests will investigate the hypothesis that there is a synergistic
effect between low-dose sulphonylurea and augmentation of the incretin effect on the beta
cell. LOGIC will also evaluate the cohort for effect of KCNJ11 genotype on physiological
response. Participants will be consented for genotyping as part of this study.
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