search
Back to results

Cognitive Function and Electrocardiogram (ECG) During Hypoglycemia and Blockade of the Renin-angiotensin System

Primary Purpose

Type 1 Diabetes, Hypoglycemia

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Angiotensin II receptor antagonists (Candesartan)
Placebo
Sponsored by
Louise Faerch
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Type 1 Diabetes focused on measuring Type 1 diabetes, Hypoglycaemia, genetic susceptibility, Renin angiotensin system activity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 diabetes
  • Danish spoken and written
  • RAS activity score>7 - diabetes duration > 5 years
  • not pregnant and safe anticonception
  • Signed informed consent.

Exclusion Criteria:

  • Treatment with an ACE blocker
  • An ARB og a renin blocker
  • Treatment with other antihypertensive drugs
  • Severe diabetic late complications
  • Renal impairment
  • Pregnancy and breastfeeding
  • Previous reactions to study medication
  • Heart insufficiency (NYHA 3-4)\
  • Known ischaemic heart disease
  • Epilepsy
  • Alcohol and drug abuse
  • Suspicion of non-compliance,
  • Plasma potassium < 3.5 mmol/l or >5.0 mmol/l.

Sites / Locations

  • Department of Cardiology and Endocrinology, Hillerød Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Candesartan

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Cognitive function and brain cortical activity assessed by EEG

Secondary Outcome Measures

Symptoms of hypoglycaemia assessed by Edinburgh Hypoglycaemia Symptom Score questionnaire
Hormonal counter-regulatory response and substrates
Blood pressure and pulse
Cardiac conduction evaluated by a three channel digital Holter Monitor.

Full Information

First Posted
January 25, 2010
Last Updated
February 4, 2013
Sponsor
Louise Faerch
search

1. Study Identification

Unique Protocol Identification Number
NCT01116180
Brief Title
Cognitive Function and Electrocardiogram (ECG) During Hypoglycemia and Blockade of the Renin-angiotensin System
Official Title
Influence of Blockade of the Renin-angiotensin System for Preservation of Cognitive Function, Hormonal Counter-regulatory Response, Symptomatology and Cardiac Repolarisation During Hypoglycaemia in Patients With Type 1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
February 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Louise Faerch

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothesis: Treating patients with type 1 diabetes with a certain antihypertensive drug preserve cerebral function during hypoglycaemia. Background: Studies have found that certain genetic variations leaves a subject with type 1 diabetes more prone to hypoglycaemia. It it thought to be a decline in cognition during hypoglycaemia that leaves them at risk of severe hypoglycaemia. The idea is tha when you suppress the genetic phenotype with a well known antihypertensive drug an improvement in cognition will occur and this will remove the patients tendency to severe hypoglycaemia. Methods: The investigators want to explore whether the cerebral function is improved during hypoglycaemia in subjects with type 1 diabetes and the above mentioned genetic variation when treated with the antihypertensive drug Candesartan.
Detailed Description
We will include 25 type 1 diabetic patients from our outpatient clinic. They are already genotyped from another trial. Each patient goes through two cycles with hyperinsulinemic glucose clamp induced hypoglycemia. The study is double blinded, randomised and placebocontrolled so the patients receive both Candesartan and placebo but in different cycles. In each cycle patients will receive either Candesartan or placebo for 7 days. After 8 days patients undergo a hypoglycaemic clamp during which primary and secondary endpoints will be measured. In the hyperinsulinemic hypoglycaemic clamp the patients will undergo an adjustment period towards euglycaemia. A period of approximately 1 hour of euglycemia, an hour of hypoglycemia and a period of recovery towards euglycemia. In each of these glycemic states primary and secondary outcomes will be measured.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes, Hypoglycemia
Keywords
Type 1 diabetes, Hypoglycaemia, genetic susceptibility, Renin angiotensin system activity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Candesartan
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Angiotensin II receptor antagonists (Candesartan)
Other Intervention Name(s)
Blopress, Atacand, Amias, Ratacand
Intervention Description
Seven days of treatment with Candesartan 32 mg, capsules.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo Capsule matching the active comparator. Given for 7 days once daily.
Primary Outcome Measure Information:
Title
Cognitive function and brain cortical activity assessed by EEG
Time Frame
2 month
Secondary Outcome Measure Information:
Title
Symptoms of hypoglycaemia assessed by Edinburgh Hypoglycaemia Symptom Score questionnaire
Time Frame
2 month
Title
Hormonal counter-regulatory response and substrates
Time Frame
2 month
Title
Blood pressure and pulse
Time Frame
2 month
Title
Cardiac conduction evaluated by a three channel digital Holter Monitor.
Time Frame
2 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 1 diabetes Danish spoken and written RAS activity score>7 - diabetes duration > 5 years not pregnant and safe anticonception Signed informed consent. Exclusion Criteria: Treatment with an ACE blocker An ARB og a renin blocker Treatment with other antihypertensive drugs Severe diabetic late complications Renal impairment Pregnancy and breastfeeding Previous reactions to study medication Heart insufficiency (NYHA 3-4)\ Known ischaemic heart disease Epilepsy Alcohol and drug abuse Suspicion of non-compliance, Plasma potassium < 3.5 mmol/l or >5.0 mmol/l.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ulrik Pedersen-Bjergaard, MD, MDSc.
Organizational Affiliation
Hillerød Hospital, Department of Cardiology and Endocrinology, Dyrehavevej 29, 3400 Hillerød
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Louise Færch, MD
Organizational Affiliation
Hillerød Hospital, Department of Cardiology and Endocrinology, Dyrehavevej 29, 3400 Hillerød
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Birger Thorsteinsson, Prof DMSc MD
Organizational Affiliation
Hillerød Hospital, Department of Cardiology and Endocrinology, Dyrehavevej 29, 3400 Hillerød. University of Copenhagen
Official's Role
Study Director
Facility Information:
Facility Name
Department of Cardiology and Endocrinology, Hillerød Hospital
City
Hillerød
ZIP/Postal Code
3400
Country
Denmark

12. IPD Sharing Statement

Learn more about this trial

Cognitive Function and Electrocardiogram (ECG) During Hypoglycemia and Blockade of the Renin-angiotensin System

We'll reach out to this number within 24 hrs