User Satisfaction Using the ADI Insulin Pump

Evaluation of User Satisfaction Using the ADI Insulin Pump

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00797771

Enrollment

Registered

2008-11-25

Start date

2008-12-31

Completion date

2010-01-31

Last updated

2011-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes

Keywords

Insulin delivery

Brief summary

Approximately 250,000 people worldwide are currently being treated with an insulin pump. This number is growing dramatically as these devices become smaller and more user-friendly. Insulin pumps allow for tight metabolic control and lifestyle flexibility while minimizing the number of hypoglycemic events. The NiliMedix ADI Insulin Pump is an ambulatory, battery operated, rate programmable micro- infusion pump, designed for continuous delivery of insulin. A custom reservoir is driven by the pressure of insulin within it to deliver preset basal profiles and patient programmed bolus of insulin through custom infusion sets, into subcutaneous tissue. This type of device requires extensive user interaction and education in order to ensure its safety. This study was designed to test the independent home-use of the NiliMedix ADI Insulin Pump, and to evaluate user's satisfaction.

Interventions

DEVICEAdi Insulin pump

insulin delivery will be defined by the physician

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Male/female age 18 years and up. * Subject is diagnosed as Type 1 Diabetes. * Pump Users for at least 6 months * HbA1c: less than 8.5% * Capable of reading pump screens in English. * Subject understands the study procedure. * Subject is willing to sign the informed consent form and comply with the study requirements.

Exclusion criteria

* Major physical, motor, mental, behavioral, or psychiatric limitations. * Subject experienced a severe hypoglycemic episode that led to hospitalization during the last 6 months. * Subject experienced an episode of Ketoacidosis during the last 6 months, while using an insulin pump. * Concurrent additional major illness. * Subject objects to the study protocol. * Physician objection * Concurrent participation in other study.

Design outcomes

Primary

Measure	Time frame
User satisfaction regarding the Adi pump functioning will be evaluated by questionnaire. The questionnaire will be administrated during the last study visit	End of study

Secondary

Measure	Time frame
Number of severe hypoglycemic events	during the study

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026