Clinical Effectiveness of Advanced Hybrid Closed-loop Systems for Achieving Time in Tight Range Among T1D Patients (TightT1)

March 17, 2026 updated by: Castilla-La Mancha Health Service

Clinical Effectiveness of Advanced Hybrid Closed-loop Systems (AHCL) for Achieving Time in Tight Range (TiTR) of Interstitial Glucose Among Adult Type 1 Diabetes (T1D) Patients

Diabetes is a chronic disease with a relevant public health burden. Maintaining blood glucose levels as close to normal as possible is essential to avoid the associated microvascular and macrovascular complications. Therefore, the key to prevent and/or reduce the development of these chronic complications lies in an adequate and strict glycemic control.

This study consist of a cross-sectional observational study among adult patients with type 1 diabetes (T1D). The main objective is to analyze the effect on time in tight range (TiTR, 70-140 mg/dL) of interstitial glucose between three different advanced hybrid closed-loop (AHCL) systems.

Study Overview

Status

Completed

Detailed Description

Diabetes is a chronic disease with a relevant public health burden. Type 1 diabetes (T1D) is characterized by the autoimmune destruction of insulin-producing pancreatic beta cells, which requires the administration of exogenous insulin for its treatment. Maintaining blood glucose levels as close to normal as possible is essential to avoid the associated microvascular and macrovascular complications that affect quality of life, as well as morbidity and mortality due to the deleterious long-term effects of suboptimal control. Therefore, the key to prevent and/or reduce the development of these complications lies in adequate and strict glycemic control.

The use of advanced hybrid closed-loop (AHCL) systems in patients with T1D is associated with improved glycemic control and quality of life in both controlled clinical trials and real-life studies. Since 2021, AHCL systems are considered the standard of care, ahead of traditional MDI.

There are three main types of AHCL systems marketed in Spain: SmartGuard in Medtronic Minimed 780G (MM780G), Control-IQ in Tandem T Slim X2 (TTSX2) and CamAPS in Ypsopump (CamAPS).

All three systems have been shown indepently to significantly improve glycaemic control in people with DM1 as expressed by the classic control targets of the International Time in Range Consensus (percentage of interstitial glucose time in range 70-180 mg/dL >70%). So much so that it has been suggested to further intensify the possible glucose targets in patients treated with AHCL systems to a time in tight range (TITR) of interstitial glucose (70-140 mg/dL) >50%.

However, there is little information on the benefits and safety of using tighter control targets. Furthermore, there is no evidence about comparing the clinical benefit differences between these three types of technology.

The main objective is to analyze the effect on time in tight range (TiTR, 70-140 mg/dL) of interstitial glucose between three different advanced hybrid closed-loop (AHCL) systems among adult people with T1D.

This is multicenter (3 centers) cross-sectional observational clinical study (non-randomized). The target population will be adult T1D patients treated with any of the aforementioned AHCL systems followed in any of the three participant centers.

Study Type

Observational

Enrollment (Actual)

189

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Badajoz
      • Badajoz, Badajoz, Spain, 06080
        • Badajoz University Hospital
    • Barcelona
      • Terrassa, Barcelona, Spain, 08221
        • Hospital Universitario Mutua de Tarrasa
    • Ciudad Real
      • Ciudad Real, Ciudad Real, Spain, 13005
        • Ciudad Real General University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adult patients with type 1 diabetes treated with AHCL attended in any of the three centers.

Description

Inclusion Criteria:

  • Patients with type 1 diabetes.
  • Age greater than or equal to 18 years.
  • Treated with advanced hybrid closed-loop systems (AHCL) for at least 3 months
  • Actived continuous glucose monitoring data in the last 14 days.

Exclusion Criteria:

  • Other types of diabetes.
  • Receiving treatment with insulin regimens other than AHCL.
  • Having received AHCL treatment for less than 3 months in a row prior to inclusion in the study with the same system.
  • No data on use of the AHCL system during the previous 14 days.
  • Severe or uncontrolled psychiatric disorder.
  • Pregnancy or end of pregnancy less than 3 months ago or preparation for pregnancy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
MM780G
Patients with type 1 diabetes treated with Medtronic Minimed 780G hybrid closed-loop systems
SmartGuard in Medtronic Minimed 780G advaced hybrid closed-loop
Other Names:
  • Medtronic Minimed 780G
TTSX2
Patients with type 1 diabetes treated with Tandem T Slim X2 hybrid closed-loop system
Control-IQ in Tandem T Slim X2 advanced hybrid closed-loop
Other Names:
  • Tandem T Slim X2
CamAPS
Patients with type 1 diabetes treated with CamAPS hybrid closed-loop system
CamAPS Fx in Ypsopump advanced hybrid closed-loop
Other Names:
  • CamAPS Fx

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
TiTR
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time in tight range (TiTR, 70-140 mg/dL) of interstitial glucose.
Retrospective data from the last 14 days after study entry

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
TIR
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time in range (TIR, 70-180 mg/dL) of interstitial glucose.
Retrospective data from the last 14 days after study entry
TAR1
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time above range 1 (180-250 mg/dL) of interstitial glucose.
Retrospective data from the last 14 days after study entry
TAR2
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time above range 2 (>250 mg/dL) of interstitial glucose.
Retrospective data from the last 14 days after study entry
TBR1
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time bellow range 1 (<70 mg/dL) of interstitial glucose.
Retrospective data from the last 14 days after study entry
TBR2
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time bellow range 2 (<55 mg/dL) of interstitial glucose.
Retrospective data from the last 14 days after study entry
HbA1C
Time Frame: Retrospective data from the last 3 months after study entry
Differences in HbA1C values (%)
Retrospective data from the last 3 months after study entry
AHCL use
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in time of use of the AHCL system (%)
Retrospective data from the last 14 days after study entry
Insulin use
Time Frame: Retrospective data from the last 14 days after study entry
Daily dose of insulin use in AHCL system (UI/day)
Retrospective data from the last 14 days after study entry
Coefficient of variation
Time Frame: Retrospective data from the last 14 days after study entry
Percentage differences in the coefficient of variation of interstitial glucose (%)
Retrospective data from the last 14 days after study entry
Quality-of-life questionnaire designed for diabetes mellitus (EsDQOL)
Time Frame: Retrospective quality-of-life during the last 3 months
Assessing the perceived quality of life according to the EsDQOL questionnaire (with values between 46 and a maximum of 230, the higher the score the poorer the satisfaction with ACHL treatment).
Retrospective quality-of-life during the last 3 months
Hypoglycemia Fear Survey (HFS questionnaire)
Time Frame: Retrospective fear to hypoglycemia during the last 3 months
Assessing the fear of hypoglycemia according to the HFS questionnaire (with values between 24 points and a maximum of 120 points, the higher the score the higher the fear of hypoglycemia).
Retrospective fear to hypoglycemia during the last 3 months
Clarke's questionnaire
Time Frame: Retrospective hypoglycemia awareness during the last 3 months
Assessing the awareness of hypoglycemia according to Clarke's questionnaire (with values between 0 and 8 points, a score equal or greater than four indicates hypoglycemia unawareness).
Retrospective hypoglycemia awareness during the last 3 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Differences in the Percetage of patients fullfilling the International Consensus of Time in Range
Time Frame: Retrospective data from the last 14 days after study entry
Differences in the Percetage of patients fullfilling the International Consensus of Time in Range (TAR2 <5%, TAR1 <25%, TIR >70%, TBR1 <4%, TBR2 <1%, CV>36%).
Retrospective data from the last 14 days after study entry

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jesus Moreno Fernandez, PhD, Castilla-La Mancha Health Public Service

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 27, 2025

Primary Completion (Actual)

October 1, 2025

Study Completion (Actual)

October 1, 2025

Study Registration Dates

First Submitted

February 7, 2025

First Submitted That Met QC Criteria

February 18, 2025

First Posted (Actual)

February 19, 2025

Study Record Updates

Last Update Posted (Actual)

March 19, 2026

Last Update Submitted That Met QC Criteria

March 17, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Under request and after consideration from all investigators.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

Yes

product manufactured in and exported from the U.S.

Yes

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Type 1 Diabetes (T1D)

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