Type 1 Diabetes Trial, Recruiting NCT07507708 Sponsor: Sue Brown Condition: Type 1 Diabetes
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Type 1 Diabetes Trial, Recruiting

NCT07507708
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be 18 years old or older at the time you agree to join the study.
  • You must have been diagnosed with Type 1 diabetes for more than 1 year, based on a doctor's assessment.
  • You must have used an FDA-approved automated insulin delivery (AID) system at some point in the last 6 months (regular use is not required).
  • You must have been using insulin for more than 6 months.
  • You must be willing to switch to a specific type of insulin approved for use with the study's pump, as directed by the study team.
  • You must have at least one supportive person (such as a family member or friend) who knows how to handle a severe low blood sugar emergency, can contact emergency services and the study team, and either lives with you or can reach you within about 30 minutes.
  • You must not currently be pregnant or breastfeeding.
  • If you are able to become pregnant, you must agree to use contraception during the study, and you must have a negative pregnancy test before starting; becoming pregnant or planning to become pregnant during the study would mean leaving the study.
  • You must be willing to wear a Dexcom continuous glucose monitor (CGM) throughout each phase of the study.
  • You must be willing to use the study's full system (CGM, insulin pump, and phone) during the relevant parts of the study.
  • You must be willing not to start any new non-insulin diabetes medications during the trial.
  • You must be willing to take part in all study activities, including attending in-person training sessions.
  • You must have internet access at home and be willing to upload your data when needed.
  • The study doctor must be confident that you can use all the study devices correctly and follow the study rules.
  • You must be able to read and speak English proficiently.

Who may not be able to join:

  • You are planning to start a new non-insulin diabetes medication (such as GLP-1 drugs or similar); however, if you have already been on a stable dose of one for at least a month, this may not apply (confirm with trial site).
  • You are currently taking sulfonylurea medications (a type of diabetes pill).
  • You have uncontrolled eye complications related to diabetes (such as active proliferative retinopathy) that are not being treated or are not responding to treatment.
  • You are currently taking SGLT-2 or SGLT-1/2 inhibitor medications (a type of diabetes drug) due to the risk of a serious complication called euglycemic DKA.
  • You have hemophilia or any other bleeding disorder.
  • You have had a severe low blood sugar episode involving a seizure or loss of consciousness in the last 12 months.
  • You have had a diabetic ketoacidosis (DKA) episode in the last 12 months.
  • You are currently receiving peritoneal dialysis or hemodialysis (kidney dialysis treatments).
  • You are currently being treated for adrenal insufficiency (a condition where your adrenal glands do not produce enough hormones).
  • You are currently being treated for a seizure disorder.
  • You have a thyroid condition (underactive or overactive thyroid) that is not well controlled with treatment.
  • You are currently using oral or injectable steroid medications at the time of enrollment.
  • You have a known ongoing skin sensitivity or reaction to adhesives that is not well managed.
  • You have any other condition that the study doctor believes could put you or the study at risk (confirm with trial site).
  • You are currently taking part in another interventional clinical trial.
  • Your direct supervisor at your workplace or school is involved in running this trial.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Sue A Brown, MD, University of Virginia Center for Diabetes Technology

Phone: (434) 249-6251

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Sue Brown
Registry
ClinicalTrials.gov
Start date
14 May 2026
Est. completion
31 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Time in range 70-140 mg/dL as computed by the study CGM; Time in range 70-140 mg/dL as computed by the study CGM

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov