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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00462371
Other study ID # ASB21004821
Secondary ID
Status Completed
Phase Phase 4
First received April 18, 2007
Last updated April 18, 2007
Start date January 2002
Est. completion date February 2004

Study information

Verified date April 2007
Source Erasmus Medical Center
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

Comparison between insulin pump treatment and multiple daily insulin injections in 38 children with type 1 diabetes4-16 years old. Outcome metabolic control, quality of life, impact of disease and cost effectiveness.

We hypothesised that insulin pump treatment would give a better metabolic control and quality of life.


Description:

The current standard of insulin treatment in type 1 diabetes is multiple daily insulin injection therapy (MDII). In the seventies, continuous subcutaneous insulin infusion (CSII) was introduced. CSII has been gaining popularity, perhaps because of technical advances resulting in improved patient comfort. In children five randomised studies(1-5) were completed to compare MDII and CSII. No data were gained about quality of life and impact of disease.

In our trial we focussed on quality of life next to metabolic control.

The trial was an open-labelled,randomised trial. Both efficacy and safety data were collected. The trial started with a 14 weeks run in phase, during all patients started MDII.In the following randomisation phase patients were randomised to continue MDII or to CSII.This phase lasted 14 weeks.In the phase thereafter all patients used CSII for 14 weeks. The trial was concluded by a 14 weeks allocated patient preference phase.

Patients were type 1 diabetic children 4-16 years old with poor metabolic control.hypothesis: better metabolic control in CSII, better quality of life in CSII.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date February 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 4 Years to 16 Years
Eligibility Inclusion Criteria:

- Type 1 diabetes,

- Diagnosed by the presence of IA-2,

- GAD-65 or islet cell cytoplasmatic auto antibodies,

- Daily insulin adminstration or 1 year of longer,

- Random C-peptide <200 pMol,

- Hba1c>8.0% and/or a history of repeated symptomatic hypoglycaemias,

- Attending regular school

Exclusion Criteria:

- Clinical manifest chronic complications,

- Pregnancy,

- Co-morbidity,

- Mental retardation,

- Psychiatric treatment or symptoms in child or parent,

- Insufficient Dutch language capabilities and absence of telephone at home

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Insulin pump (CSII)


Locations

Country Name City State
Netherlands ErasmusMC/Sophia´s children´s Hospital Rotterdam

Sponsors (2)

Lead Sponsor Collaborator
Erasmus Medical Center Netherlands: Ministry of Health, Welfare and Sports

Country where clinical trial is conducted

Netherlands, 

References & Publications (5)

DiMeglio LA, Pottorff TM, Boyd SR, France L, Fineberg N, Eugster EA. A randomized, controlled study of insulin pump therapy in diabetic preschoolers. J Pediatr. 2004 Sep;145(3):380-4. — View Citation

Doyle EA, Weinzimer SA, Steffen AT, Ahern JA, Vincent M, Tamborlane WV. A randomized, prospective trial comparing the efficacy of continuous subcutaneous insulin infusion with multiple daily injections using insulin glargine. Diabetes Care. 2004 Jul;27(7):1554-8. — View Citation

Fox LA, Buckloh LM, Smith SD, Wysocki T, Mauras N. A randomized controlled trial of insulin pump therapy in young children with type 1 diabetes. Diabetes Care. 2005 Jun;28(6):1277-81. — View Citation

Weintrob N, Benzaquen H, Galatzer A, Shalitin S, Lazar L, Fayman G, Lilos P, Dickerman Z, Phillip M. Comparison of continuous subcutaneous insulin infusion and multiple daily injection regimens in children with type 1 diabetes: a randomized open crossover trial. Pediatrics. 2003 Sep;112(3 Pt 1):559-64. — View Citation

Wilson DM, Buckingham BA, Kunselman EL, Sullivan MM, Paguntalan HU, Gitelman SE. A two-center randomized controlled feasibility trial of insulin pump therapy in young children with diabetes. Diabetes Care. 2005 Jan;28(1):15-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary metabolic control
Primary quality of life
Secondary cost effectiveness
Secondary surrogate markers for late complications
Secondary adverse events
Secondary impact of disease
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