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Glucagon in MODY (Maturity Onset Diabetes of the Young)

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University of Oxford

Status

Completed

Conditions

MODY1
MODY3

Treatments

Other: Omission of gliclazide

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to determine whether fasting and post-prandial glucagon secretion is suppressed by gliclazide in patients with HNF1-/4-alpha MODY. Participants will undergo an oral glucose tolerance test (OGTT) before and after omitting their gliclazide medication for 3 days.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of HNF1-alpha or HNF4-alpha MODY.
  • Currently on gliclazide treatment

Exclusion criteria

  • Currently taking any anti-diabetic medication other than gliclazide and metformin
  • Oral steroid treatment 30 days prior to the start or at any time during the study period.
  • Known malignancy or any other condition or circumstance which, in the opinion of the investigator, would affect the patient's ability to participate in the protocol.
  • Felt to be unsuitable to participate in the study in the opinion of the Chief Investigator.
  • Currently participating in a clinical trial involving an anti-diabetic medication

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Omission of gliclazide
Experimental group
Treatment:
Other: Omission of gliclazide

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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