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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06338072
Other study ID # DIABETEXX/1
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 3, 2024
Est. completion date August 1, 2025

Study information

Verified date April 2024
Source Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this observational study is to assess the effectiveness of automatic insulin infusion in responding to changes in insulin sensitivity throughout various phases of the menstrual cycle in a cohort of reproductive-aged women with type 1 diabetes, using an advanced closed-loop system. By gaining insights into both the limitations and effectiveness of this adaptation, we aim to inform the enhancement of control algorithms and learning strategies within closed-loop systems. This research is especially vital for addressing the distinct challenges that women commonly encounter in maintaining glycemic control.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 119
Est. completion date August 1, 2025
Est. primary completion date January 1, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Diagnostic criteria for DM1 according to ADA - Women and men treated with the Medtronic© MinimedTM 780G advanced closed loop system. - Women presenting spontaneous regular menstrual cycles with a duration of 24 to 35 days, during the last year. - Men under 50 years old. - Acceptance of participation in the study and signing of the informed consent Exclusion Criteria: - Gestation - Use of hormonal contraceptives (including intrauterine devices) - Institutionalization, serious or terminal illness or renal replacement therapy. - Refusal to participate in the study or to sign the informed consent

Study Design


Locations

Country Name City State
Spain Lía Nattero-Chávez Madrid

Sponsors (2)

Lead Sponsor Collaborator
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal Universitat Politècnica de València

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time in range To assess the influence of menstrual cycle phases on the glycemic control expressed as time in range (% of time between 70-180 mg/dl of interstitial glucose). 1 month
Secondary Time below range To assess the influence of menstrual cycle phases on the glycemic control expressed as time in below range (% of time < 70 mg/dl of interstitial glucose). 1 month
Secondary Time above range To assess the influence of menstrual cycle phases on time in above range (% of time >180 mg/dl of interstitial glucose). 1 month
Secondary Caloric intake To assess the influence of changes in intake throughout the menstrual cycle 1 month
Secondary Temperature To collect temperature using a wearable. 1 month
Secondary Photoplethysmography To collect photoplethysmography using a wearable. 1 month
Secondary Accelerometry To collect acelerometry using a wearable. 1 month
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