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NCT01474538 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy Study of Insulin Lispro Versus Insulin Aspart in Participants With Type 2 Diabetes on Insulin Pump Therapy

A Phase 3 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 3
Development phase
122
Enrollment target

NCT01474538: Completed Phase 3 study, sponsored by Eli Lilly and Company.

NCT01474538 is a Phase 3 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 122 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01474538, a Phase 3 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 3
Development phase
122 participants
Enrollment target

Study Summary

This study will provide information on the use of insulin lispro and insulin aspart in insulin pumps in participants with type 2 diabetes.

Primary Outcome

Hemoglobin A1c (HbA1c) is a form of hemoglobin which is measured primarily to identify the average plasma glucose concentration over the last 8-12 weeks. Least Squares (LS) means were adjusted for treatment, period, sequence, thiazolidinedione use (Yes/No), baseline HbA1c (\>8% or ≤8%) and participants.

Interventions

  • DRUG Insulin Lispro
  • DRUG Insulin Aspart

Trial Details

FieldValue
Enrollment Target 122 participants
Start Date 2011-12
Est. Completion 2013-02
Phase Phase 3
Eli Lilly and Company

1,341 total trials

What the finished NCT01474538 record still lists

NCT01474538 is an interventional study that assigns participants to a tested intervention. The registered 122 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 2 interventions - of which Insulin Lispro is the first listed.

NCT01474538 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01474538 about?

NCT01474538 is a clinical study titled "Safety and Efficacy Study of Insulin Lispro Versus Insulin Aspart in Participants With Type 2 Diabetes on Insulin Pump Therapy". This study will provide information on the use of insulin lispro and insulin aspart in insulin pumps in participants with type 2 diabetes.

What is the current status of trial NCT01474538?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 122 participants. The study started on 2011-12. Estimated completion is 2013-02.

What interventions are being tested in trial NCT01474538?

The interventions under investigation include: Insulin Lispro (DRUG), Insulin Aspart (DRUG).

Who is sponsoring clinical trial NCT01474538?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01474538's enrollment target sits among peer trials

122 1617th of 2000 higher than 382 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT01474538, the US trial registry maintained by the National Library of Medicine. NCT01474538 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.