Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00325559
Other study ID # 1122
Secondary ID
Status Completed
Phase N/A
First received May 12, 2006
Last updated January 12, 2011
Start date June 2006

Study information

Verified date January 2011
Source University Hospital Inselspital, Berne
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Interventional

Clinical Trial Summary

This study aims at investigating the effect of hyperglycaemia on physical performance and local energy stores in the muscle in patients with type 1 diabetes mellitus under exercise conditions.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date
Est. primary completion date March 2007
Accepts healthy volunteers
Gender Male
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Male

- Aged from 20 to 40 years

- Patients with type 1 diabetes mellitus lasting for at least 5 years (C-Peptide = 0.3 nmol/l in the presence of a plasma glucose level = 7 mmol/L, indicating insulin dependence)

- Insulin delivery by CSII (continuous subcutaneous insulin infusion) for at least 6 months

- Acceptable to good metabolic control, reflected by an HbA1c 5-8%

- Normal insulin sensitivity, reflected by a daily insulin requirement of 0.3-1.0 U/kg body weight

- minimum 30' of moderate exercise 3 times per week

- BMI in the range of 18-25 kg/m2

Exclusion Criteria:

- Chronic complications of diabetes:

- Microalbuminuria (Mogensen nephropathy stadium = III)

- Sensory neuropathy (vibration better than 5/8 at the metatarsophalangeal articulation of digitus I)

- Proliferating retinopathy

- No history of macro-vascular complications

- Clinically relevant autonomous neuropathy

- Smoking

- Abnormal thyroid function

- Major depression, psychosis and other severe personality disorders, claustrophobia

- Active neoplasia

- Contraindications to exposure to a 1.5 T magnetic field (pace-makers, osteosynthetic material, etc.)

- Abnormal liver or renal function (creatinine > 130 µmol/L; ASAT and ALAT > 3 times the upper reference limit)

- Excessive alcohol consumption (>60g/d) or drug-abuse

- Refusal to give written informed consent

- Participation in another study

- Patients, who are not suitable for the study according to the study physician

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind


Intervention

Procedure:
Normoinsulinemic eu- or hyperglycemic clamp


Locations

Country Name City State
Switzerland Department of Endocrinology, Diabetes and Clinical Nutrition, University Hospital Bern

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Inselspital, Berne

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Paired difference in the time to complete a time trial corresponding to 5 km cycling between euglycaemia and hyperglycaemia
Secondary Muscle glycogen content during exercise in the working muscle (pre test vs. post test), in euglycaemia and hyperglycaemia respectively (All following endpoints are paired differences (euglycaemia vs. hyperglycaemia) of paired differences (pre
Secondary IMCL content during exercise in the working muscle
Secondary Rate of appearance of glucose
Secondary Rate of disappearance of glucose
Secondary Rate of glucose infusion
Secondary Total glucose oxidation
Secondary Oxidation of endogenous glucose
Secondary Oxidation of exogenous glucose
Secondary Fat oxidation (calculated via tracer and via RER)
Secondary Rate of perceived exertion
Secondary Serum lactate levels during the exercise test
Secondary Amino acid oxidation
Secondary Serum free fatty acid concentration
Secondary Serum insulin levels
Secondary Serum glucose levels
Secondary Time to achieve hyperglycemia during clamp
Secondary Pretest diary data
See also
  Status Clinical Trial Phase
Completed NCT04030091 - Pulsatile Insulin Infusion Therapy in Patients With Type 1 and Type 2 Diabetes Mellitus Phase 4
Terminated NCT03605329 - Evaluation of the Severity of Cardiovascular Autonomic Neuropathy in Type 1 Diabetic Patients With OSAS N/A
Completed NCT01696266 - An International Survey on Hypoglycaemia Among Insulin-treated Patients With Diabetes
Recruiting NCT06050642 - Study of the Impact of PROximity Support for Patients With Type 1 DIABetes Treated With an Insulin Pump or Closed Loop. N/A
Completed NCT05107544 - Metabolic, Physical Fitness and Mental Health Effects of High Intensity Interval Training (HIIT) in Adolescents With Type 1 Diabetes N/A
Active, not recruiting NCT04443153 - Adapting Diabetes Treatment Expert Systems to Patient in Type 1 Diabetes N/A
Completed NCT04521634 - Glycaemic Variability in Acute Stroke
Completed NCT04569994 - A Study to Look at the Safety of NNC0363-0845 in Healthy People and People With Type 1 Diabetes Phase 1
Completed NCT04089462 - Effects of Frequency and Duration of Exercise in People With Type 1 Diabetes A Randomized Crossover Study N/A
Completed NCT03143816 - Study Comparing Prandial Insulin Aspart vs. Technosphere Insulin in Patients With Type 1 Diabetes on Multiple Daily Injections: Investigator-Initiated A Real-life Pilot Study-STAT Study Phase 4
Completed NCT01892319 - An International Non-interventional Cohort Study to Evaluate the Safety of Treatment With Insulin Detemir in Pregnant Women With Diabetes Mellitus. Diabetes Pregnancy Registry
Recruiting NCT04039763 - RT-CGM in Young Adults at Risk of DKA N/A
Completed NCT04042207 - Diabeloop for Highly Unstable Type 1 Diabetes N/A
Not yet recruiting NCT06068205 - COMPARATIVE ANALYSIS OF THE MORPHO-MECHANICAL PROPERTIES OF RED BLOOD CELLS EXTRACTED FROM DIABETIC PATIENTS WITH AND WITHOUT MICROVASCULAR COMPLICATIONS
Recruiting NCT05909800 - Prolonged Remission Induced by Phenofibrate in Children Newly Diagnosed With Type 1 Diabetes. Phase 2
Active, not recruiting NCT04974528 - Afrezza® INHALE-1 Study in Pediatrics Phase 3
Completed NCT04530292 - Home Intervention and Social Precariousness in Childhood Diabetes N/A
Completed NCT05428943 - OPT101 in Type 1 Diabetes Patients Phase 1
Recruiting NCT03988764 - Monogenic Diabetes Misdiagnosed as Type 1
Completed NCT05597605 - The SHINE Study: Safety of Implant and Preliminary Performance of the SHINE SYSTEM in Diabetic Subjects N/A