Single Arm Intervention Trial of DEKA TWIIST TM Insulin Pump Utilizing Tidepool Loop Algorithm in Pregnant People With Pre-existing Type 1 Diabetes

NCT07808385 | Not Yet Recruiting DMC FDA Device

• 1 other identifier: 25-011927
• Study Type: interventional
• Target: 32
• Locations: 1 country
• Sites: 4

Brief Summary

Suboptimal glycemic control during pregnancy contributes to adverse maternal and fetal health outcomes and previous automated insulin delivery (AID) studies have demonstrated improvement in glucose control across all ages and sexes irrespective of past treatment modality or diabetes duration with no increase in hypoglycemia. However, very few studies evaluating AID system use in pregnancy have been performed in the US and no AID systems are currently approved for use during pregnancy. The objective of this trial is to evaluate the safety and efficacy of THE TWIIST™ system that enables the selection of pregnancy-specific glucose targets. This phase 3 pivotal trial will assess the system's performance in pregnant people with pre-existing type 1 diabetes in the US, starting as early as pregnancy confirmation, continuing throughout the pregnancy including delivery and up to 6 weeks post-partum.

Conditions

Type 1 Diabetes; Pregnancy

Outcome Measures

Primary Outcomes (1)

• Time in Range 60-140 mg/dL per night

  30 weeks

Study Arms (1)

AID and CGM

EXPERIMENTAL

Device: Automated Insulin Delivery (AID)

Interventions

Automated Insulin Delivery (AID) DEVICE

The AID control algorithm, that will be used during the study employs a model-based predictive control algorithm to forecast future glucose levels. This predictive model accounts for the impact of delivered insulin, user-entered carbohydrates, and incorporates two short-term adaptations: "glucose momentum" and "retrospective correction." These features work to optimize glucose management with precision. The impact of carbohydrates is calculated based on the user-defined insulin-to-carbohydrate ratio and insulin sensitivity factor (ISF), while the insulin effect is governed by the ISF itself. The system then dynamically adjusts insulin delivery, aiming to bring glucose levels in line with the midpoint of the user's personalized glucose target range. Loop fine-tunes insulin delivery by increasing or decreasing the basal insulin rate, as needed, each time a new CGM value is received.

AID and CGM

Eligibility Criteria

• Age: 18 Years - 45 Years
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Singleton pregnancy is confirmed by ultrasound.
• Pregnant woman between pregnancy confirmation to 96/7 weeks gestation.
• Clinical diagnosis of T1D for 1 year or longer.
• Using insulin pump (AID/SAP) or multiple daily insulin injections at screening visit.
• Willing to use U100 aspart (Novolog) or lispro (Humalog) insulin during the study.
• Willing to announce all carbohydrate intake unless for the treatment or prevention of hypoglycemia.
• No significant maternal and/or fetal complications at the time of enrollment visit.
• Willing to abide by study protocol.
• Willing to learn and use study-provided devices and perform necessary actions for interacting with devices when needed.
• Able and willing to receive routine and specialty obstetric care during the study.
• Able to speak and understand English and provide informed consent.
• Able to have at least one care partner available during the study. A care partner is defined as an adult person (≥18 yrs.) who will either be staying in the same location as the participant or within a 40-mile radius and willing to be trained on study devices and using the TWIIST smartphone App (follower app), will to provide treatment of hypo- and hyperglycemia, and able to take the participant to the hospital or call 911 (emergency services) in case of an emergency.

You may not qualify if:

• Individuals with T2D, gestational diabetes, or other types of diabetes (e.g., CFRD, MODY, etc.).
• Use of basal insulin alone.
• Use of short-acting insulin alone, unless use is through an insulin pump.
• Severe allergy to medical grade adhesives within the last 3 months that would inhibit participant ability to wear the study devices.
• Significant maternal and/or fetal complications, such as pre-existing heart disease (untreated or unstable cardiac diseases), pre-existing severe kidney (eGFR \< 45) disease and any other condition that limits participant safety as per investigator discretion.
• Unwilling to wear the study insulin pump for the duration of the study or unwilling to switch from current insulin therapy to investigational device for duration of the study.
• Presence of significant skin diseases/changes at sensor or infusion wear sites (for example: extensive scarring, extensive eczema, dermatitis herpetiformis, extensive burn or extensive psoriasis).
• Multifetal pregnancy.
• Inadequate access to a phone and/or computer (for downloading devices and web-based communications).
• Unable to attend required on-site study visits due to a planned move to a non-commutable distance to the study site.
• People with advanced diabetes complications such as advanced nephropathy (creatinine \>1.5 mg/dl, eGFR \<45 or currently on dialysis), severe autonomic neuropathy, uncontrolled gastroparesis, advanced retinopathy requiring active treatments or as per investigator judgment.
• Any bleeding disorder or hemophilia.
• Abnormal TSH 6 weeks after two consecutive titrations of thyroid medications
• Adrenal insufficiency.
• History of severe hypoglycemic event or DKA requiring hospitalization in the past 3 months or greater than 1 episode of DKA within the last year.

Sponsors & Collaborators

• Mayo Clinic: lead
• Icahn School of Medicine at Mount Sinai: collaborator
• University of Colorado, Denver: collaborator
• Stanford University: collaborator

Study Sites (4)

Stanford University

Stanford, California, 94305, United States

Location

University of Colorado, Anschutz Medical Campus

Aurora, Colorado, 80045, United States

Location

Mayo Clinic

Rochester, Minnesota, 55905, United States

Location

Icahn School of Medicine at Mount Sinai

New York, New York, 10029, United States

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 1

Condition Hierarchy (Ancestors)

Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases; Autoimmune Diseases; Immune System Diseases

Study Officials

• Yogish C. Kudva, MBBS

  Mayo Clinic

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Chloe Miller, BS

CONTACT

507-255-0316; miller.Chloe4@mayo.edu

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: September 2, 2026
• First Posted: September 8, 2026
• Study Start: September 1, 2026
• Primary Completion (Estimated): May 1, 2027
• Study Completion (Estimated): December 1, 2028
• Last Updated: September 8, 2026

Record last verified: 2026-09

Locations

US (4)