Recurrent Hypoglycaemia in Type 1 Diabetes (HypoNeuro)
Primary Purpose
Hypoglycaemia
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Insulin clamp
Sponsored by
About this trial
This is an interventional prevention trial for Hypoglycaemia focused on measuring Diabetes, Hypoglycaemia, EEG, Thermography, Hypoglycaemia-associated autonomic failure, QTc interval, Hypoglycemic alarm device, Hormone response
Eligibility Criteria
Inclusion Criteria:
- Type 1 diabetes
- Age > 18 years
- - Have had diabetes for more than 5 years
- Negative pregnancy test
- Caucasian
- Signed written informed consent
Exclusion Criteria:
- Pregnant or breastfeeding
- Epilepsy
- Self-perceived impaired hearing
- Use of antiepileptic medicine
- Use of neuroleptics within the last 6 months
- Use of benzodiazepines within the last month
- Use of betablockers
- Previous stroke or other disease in the brain
- Cardiovascular disease
- Alcohol-, drug- or medicine abuse
- Previous allergic reaction to heparin
Sites / Locations
- Hillerod Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Patients with hypoglycemia awareness
patients with hypoglycaemic unawareness.
Arm Description
Patients who have symptoms when the blood sugar level is low
Patients who do not feel any symptoms when the blood sugar levels are low
Outcomes
Primary Outcome Measures
EEG
EEG will be analysed in order to see whether there are any differences between aware and unaware patients during hypoglycaemia. It is our hope that the result can help develop an alarm before the patient experiences severe hypoglycaemia.
Secondary Outcome Measures
QTc interval
The investigators want to investigate whether the QTc complex gets wider during hypoglycaemia. This is in order to see whether long QTc could be the explanation behind sudden dearth in diabetes patients.
Skin temperature
Skin temperature will be measured by thermography. The investigators want to see whether the skin can be used as a biomarker for hypoglycaemia.
Auditory evoked potentials
The investigators what to see whether there is any difference in auditory evoked potentials (AEP) between aware and unaware diabetic patients. The subject will hear a common and a rare sound in a 4:1 ratio while the EEG is recorded. Afterwards the data is analyzed and the AEPs are addressed.
Cognitive function
The investigators want to address whether there are any differences in the cognitive function between aware and unaware patients. The cognitive function will be addressed by the use of cognitive function tests (CalCAP) and Stroops tests as well.
Full Information
NCT ID
NCT01337362
First Posted
March 30, 2011
Last Updated
October 15, 2014
Sponsor
Hillerod Hospital, Denmark
Collaborators
University of Southern Denmark, Rigshospitalet, Denmark, UNEEG Medical A/S
1. Study Identification
Unique Protocol Identification Number
NCT01337362
Brief Title
Recurrent Hypoglycaemia in Type 1 Diabetes
Acronym
HypoNeuro
Official Title
Recurrent Hypoglycaemia in Type 1 Diabetes: Effects on Cognitive Function, Cerebral Electrical Activity, and Skin Temperature
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hillerod Hospital, Denmark
Collaborators
University of Southern Denmark, Rigshospitalet, Denmark, UNEEG Medical A/S
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with type 1 diabetes are at risk of very low blood sugar levels (hypoglycaemia) as a severe side effect to insulin therapy, in particular subjects who have lost warning of hypoglycaemia. During hypoglycaemia a low frequent activity can be seen with electroencephalography (EEG) as cognitive function declines.
The purpose of the study is to investigate the activity in the brain, the cognitive function, and the skin temperature when patients are exposed to repeated hypoglycaemia. The results will show whether the response to hypoglycaemia will change after repeated episodes.
It is our hope that results can contribute to improved understanding of hypoglycaemic EEG changes.
Detailed Description
Background:
Patients with type 1 diabetes are at risk of severe hypoglycaemia as a severe side effect to insulin therapy, in particular subjects who have lost warning of hypoglycaemia (hypoglycaemia unawareness). The episodes are associated with impaired quality of life and can lead to permanent brain damage and death.
During hypoglycaemia a low frequent activity can be seen with electroencephalography (EEG) as cognitive function declines. Repeated hypoglycaemic episodes result in down regulation of counter regulatory and symptomatic responses. It is not known whether a similar phenomenon is present for cerebral dysfunction as judged by EEG changes and cognitive function.
The purpose is to investigate the activity in the brain, the cognitive function, and the skin temperature when patients are exposed to repeated hypoglycaemia. The results will show whether the response to hypoglycaemia will change after repeated episodes.
The methods:
The investigators will recruit two groups of patients: Patients with hypoglycemia awareness and patients with hypoglycaemic unawareness.
The patients are exposed to hypoglycaemia on two concomitant days while the investigators record EEG and perform cognitive tests. Skin temperature is assessed by the use of thermography. If the patient has hypoglycaemic unawareness a 4 week period follows where the glycaemic control is loosened to avoid hypoglycaemia episodes and the patients is then exposed to hypoglycaemia again.
The prospect:
It is the investigators hope that results can contribute to improved understanding of hypoglycaemic EEG changes and skin temperature changes. This could be of potential benefit for patients with hypoglycaemic unawareness.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoglycaemia
Keywords
Diabetes, Hypoglycaemia, EEG, Thermography, Hypoglycaemia-associated autonomic failure, QTc interval, Hypoglycemic alarm device, Hormone response
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patients with hypoglycemia awareness
Arm Type
Active Comparator
Arm Description
Patients who have symptoms when the blood sugar level is low
Arm Title
patients with hypoglycaemic unawareness.
Arm Type
Experimental
Arm Description
Patients who do not feel any symptoms when the blood sugar levels are low
Intervention Type
Procedure
Intervention Name(s)
Insulin clamp
Other Intervention Name(s)
Insulin, clamp
Intervention Description
Patients will be exposed to low bloodsugar
Primary Outcome Measure Information:
Title
EEG
Description
EEG will be analysed in order to see whether there are any differences between aware and unaware patients during hypoglycaemia. It is our hope that the result can help develop an alarm before the patient experiences severe hypoglycaemia.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
QTc interval
Description
The investigators want to investigate whether the QTc complex gets wider during hypoglycaemia. This is in order to see whether long QTc could be the explanation behind sudden dearth in diabetes patients.
Time Frame
2 years
Title
Skin temperature
Description
Skin temperature will be measured by thermography. The investigators want to see whether the skin can be used as a biomarker for hypoglycaemia.
Time Frame
2 years
Title
Auditory evoked potentials
Description
The investigators what to see whether there is any difference in auditory evoked potentials (AEP) between aware and unaware diabetic patients. The subject will hear a common and a rare sound in a 4:1 ratio while the EEG is recorded. Afterwards the data is analyzed and the AEPs are addressed.
Time Frame
2 years
Title
Cognitive function
Description
The investigators want to address whether there are any differences in the cognitive function between aware and unaware patients. The cognitive function will be addressed by the use of cognitive function tests (CalCAP) and Stroops tests as well.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 1 diabetes
Age > 18 years
- Have had diabetes for more than 5 years
Negative pregnancy test
Caucasian
Signed written informed consent
Exclusion Criteria:
Pregnant or breastfeeding
Epilepsy
Self-perceived impaired hearing
Use of antiepileptic medicine
Use of neuroleptics within the last 6 months
Use of benzodiazepines within the last month
Use of betablockers
Previous stroke or other disease in the brain
Cardiovascular disease
Alcohol-, drug- or medicine abuse
Previous allergic reaction to heparin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne-Sophie Sejling, MD
Organizational Affiliation
Hillerod Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hillerod Hospital
City
Hillerød
ZIP/Postal Code
3400
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
26745007
Citation
Rubega M, Sparacino G, Sejling AS, Juhl CB, Cobelli C. Hypoglycemia-Induced Decrease of EEG Coherence in Patients with Type 1 Diabetes. Diabetes Technol Ther. 2016 Mar;18(3):178-84. doi: 10.1089/dia.2015.0347. Epub 2016 Jan 8.
Results Reference
derived
Learn more about this trial
Recurrent Hypoglycaemia in Type 1 Diabetes
We'll reach out to this number within 24 hrs