Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01112696 · ClinicalTrials.gov registry record · NA

An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor

A NA study, sponsored by Medtronic MiniMed.

Completed
Registry status
NA
Development phase
100
Enrollment target

NCT01112696: Completed NA study, sponsored by Medtronic MiniMed.

NCT01112696 is a NA study that has completed, run by Medtronic MiniMed. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01112696, a NA study, has completed, sponsored by Medtronic MiniMed.

COMPLETED
Registry status
NA
Development phase
100 participants
Enrollment target

Study Summary

The purpose of the study is to assess the performance of a new subcutaneous glucose sensor over a seven-day sensor life when used with currently marketed Medtronic Diabetes devices. In addition performance will be calculated for use of the new sensor with proposed new devices using new calibration algorithms.

Primary Outcome

The primary accuracy parameter (primary effectiveness endpoint) was the comparative readings of paired sensor and YSI glucose readings, measured on days 1 through 6. Accuracy is defined as within 20% agreement between YSI and paired sensor (within 20 mg/dL if YSI \<80 mg/dL). Accuracy ranges from 0 - 100, with higher number suggests better accuracy.

Interventions

  • DEVICE Sensor wear

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2010-04
Est. Completion 2010-11
Phase NA
Medtronic MiniMed

29 total trials

What the finished NCT01112696 record still lists

NCT01112696 is an interventional study that assigns participants to a tested intervention. The registered 100 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 (93% lower).

The record links to 0 conditions, and to 1 intervention - of which Sensor wear is the first listed.

NCT01112696 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01112696 about?

NCT01112696 is a clinical study titled "An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor". The purpose of the study is to assess the performance of a new subcutaneous glucose sensor over a seven-day sensor life when used with currently marketed Medtronic Diabetes devices. In addition performance will be calculated for use of the new sensor with proposed new devices using new calibration a...

What is the current status of trial NCT01112696?

This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2010-04. Estimated completion is 2010-11.

What interventions are being tested in trial NCT01112696?

The interventions under investigation include: Sensor wear (DEVICE).

Who is sponsoring clinical trial NCT01112696?

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 NCT01112696's enrollment target sits among peer trials

100 840th of 2000 higher than 1,081 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01048281 · 100 participants

    Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

  • NCT01161199 · 100 participants

    The Use of Leukapheresis to Support HIV Pathogenesis Studies

  • NCT01327690 · 100 participants · Early Phase 1

    Mental Health in Veterans and Families After Group Therapies

  • NCT01730781 · 100 participants

    Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01112696, the US trial registry maintained by the National Library of Medicine. NCT01112696 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.