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NCT02003898 · ClinicalTrials.gov registry record · NA

Post Approval Study of the TS Feature With the 530G Pump System Supplemented With Commercial Patient Data

A NA study, sponsored by Medtronic MiniMed.

Completed
Registry status
NA
Development phase
372
Enrollment target

NCT02003898: Completed NA study, sponsored by Medtronic MiniMed.

NCT02003898 is a NA study that has completed, run by Medtronic MiniMed. The registered enrollment target is 372 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (74% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02003898, a NA study, has completed, sponsored by Medtronic MiniMed.

COMPLETED
Registry status
NA
Development phase
372 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the Threshold Suspend (TS) feature of the Medtronic MiniMed® 530G insulin pump in patients 16 and older with insulin requiring diabetes.

Primary Outcome

Comparison of A1C measurement from baseline to end of study in the CEP266 study population. The overall mean change in A1C from baseline will be estimated and compared by a non-inferiority test with an A1C margin of 0.4% and a significance level of 0.025 (one-sided) with the CEP 266 study population.

Interventions

  • DEVICE Medtronic MiniMed 530G Insulin Pump

Trial Details

FieldValue
Enrollment Target 372 participants
Start Date 2013-11-26
Est. Completion 2018-02-20
Phase NA
Medtronic MiniMed

29 total trials

What the finished NCT02003898 record still lists

NCT02003898 is an interventional study that assigns participants to a tested intervention. The registered 372 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (74% lower).

The record links to 0 conditions, and to 1 intervention - of which Medtronic MiniMed 530G Insulin Pump is the first listed.

NCT02003898 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02003898 about?

NCT02003898 is a clinical study titled "Post Approval Study of the TS Feature With the 530G Pump System Supplemented With Commercial Patient Data". The purpose of this study is to evaluate the Threshold Suspend (TS) feature of the Medtronic MiniMed® 530G insulin pump in patients 16 and older with insulin requiring diabetes.

What is the current status of trial NCT02003898?

This trial is currently completed. It is a NA study. The enrollment target is 372 participants. The study started on 2013-11-26. Estimated completion is 2018-02-20.

What interventions are being tested in trial NCT02003898?

The interventions under investigation include: Medtronic MiniMed 530G Insulin Pump (DEVICE).

Who is sponsoring clinical trial NCT02003898?

This trial is sponsored by Medtronic MiniMed, which has 29 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02003898's enrollment target sits among peer trials

372 280th of 2000 higher than 1,720 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02003898, the US trial registry maintained by the National Library of Medicine. NCT02003898 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.