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NCT05528770 · ClinicalTrials.gov registry record · NA

Evaluation of The Postprandial Impact of Automated Priming Bolus for Full Closed Loop Insulin Delivery

A NA study of Type 1 Diabetes, sponsored by Marc Breton.

Completed
Registry status
NA
Development phase
15
Enrollment target
1
Study location

NCT05528770: Completed NA study of Type 1 Diabetes, sponsored by Marc Breton.

NCT05528770 is a NA study of Type 1 Diabetes that has completed, run by Marc Breton. The registered enrollment target is 15 participants, below the 767-participant average among 198 other Type 1 Diabetes trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05528770, a NA study of Type 1 Diabetes, has completed, sponsored by Marc Breton.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to understand the impact of the automated priming boluses on the safety and feasibility of a new fully automated AP controller.

Primary Outcome

Percentage of CGM values falling between 70 and 180 mg/dL during daytime (6am to midnight)

Conditions Studied

Interventions

  • DEVICE FCL+BPS
  • DEVICE FCL

Study Locations (1)

Virginia

  • University of Virginia Center for Diabetes Technology - Charlottesville

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2022-10-20
Est. Completion 2023-01-15
Phase NA
Marc Breton

6 total trials

What the finished NCT05528770 record still lists

NCT05528770 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 767-participant average among 198 other Type 1 Diabetes trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Type 1 Diabetes appearing as the primary indexed condition, and to 2 interventions - of which FCL+BPS is the first listed.

NCT05528770 reports a single indexed study location in Virginia.

Frequently Asked Questions

What is clinical trial NCT05528770 about?

NCT05528770 is a clinical study titled "Evaluation of The Postprandial Impact of Automated Priming Bolus for Full Closed Loop Insulin Delivery". The purpose of this study is to understand the impact of the automated priming boluses on the safety and feasibility of a new fully automated AP controller.

What is the current status of trial NCT05528770?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2022-10-20. Estimated completion is 2023-01-15.

What conditions does trial NCT05528770 study?

This clinical trial studies the following conditions: Type 1 Diabetes.

What interventions are being tested in trial NCT05528770?

The interventions under investigation include: FCL+BPS (DEVICE), FCL (DEVICE).

Who is sponsoring clinical trial NCT05528770?

This trial is sponsored by Marc Breton, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05528770 being conducted?

This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Type 1 Diabetes

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05528770's enrollment target sits among peer trials

15 166th of 198 higher than 30 of 198 other Type 1 Diabetes trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Type 1 Diabetes 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 NCT05528770, the US trial registry maintained by the National Library of Medicine. NCT05528770 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.