Impact of the use of Extended™ Wear Infusion sets on metabolic, ultrasound, and psychological outcomes in adults with type 1 diabetes using the Medtronic MiniMed 780G: a pilot randomized controlled trial

INTRODUCTION: In people with type 1 diabetes (PwT1DM), insulin infusion sets (IIS) are often regarded as the most fragile componentof insulin pump therapy. Standard IISs should be replaced every 2-3 days to prevent site complications and hyperglycemia. The objectiveof this randomized controlled trial was to evaluate the impact of 7-day Extended™ Wear Infusion sets (EIS; Medtronic MiniMed,Northridge, CA, USA) on metabolic, ultrasound (USG), and psychological outcomes in PwT1DM treated with the MiniMed 780G system(MM780G, Medtronic MiniMed, Northridge, CA, USA). MATERIAL AND METHODS: Fifteen participants in both the intervention (EIS) and control groups (standard IIS) completed the 3-month study.One participant in the control group did not attend the follow-up USG examination; however, all other clinical, continuous glucose monitoring(CGM), and questionnaire data were available and included in the analyses. In the intervention group, the mean age was 36.1 ± 10.7years, diabetes duration 20.3 ± 7.6 years, body mass index (BMI) 24.9 ± 4.0 kg/m², and glycated hemoglobin A1c (HbA1c) 6.7 ± 0.5%. There were no significant baseline differences between groups in age, diabetes duration, CGM indices, or HbA1c. RESULTS: Across the study period, no statistically significant differences were observed between the control and intervention groups with respect to the number of lipohypertrophic lesions, the volume of the largest lesion, HbA1c, CGM indices or insulin requirements. Inboth groups (with no between-group differences), World Health Organization (WHO) 5 scores indicated improvements in psychologicalwell-being. Notably, 80% of participants reported that EIS were more comfortable than standard sets, and 73.3% stated that the newinfusion sets met their expectations. Two-thirds of participants found that the new infusion sets made life easier. CONCLUSIONS: These findings suggest that EIS are a safe and effective option for glycemic management in adults, without increasing lipohypertrophic lesions and with high patient acceptance.

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Publication Details

Journal
Endokrynologia Polska
Published
2026-09-29
DOI
https://doi.org/10.5603/ep.112819
Primary Topic
Diabetes Management and Research
Type
article
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article

Impact of the use of Extended™ Wear Infusion sets on metabolic, ultrasound, and psychological outcomes in adults with type 1 diabetes using the Medtronic MiniMed 780G: a pilot randomized controlled trial

Tomasz Klupa, Bartłomiej Matejko, Damian Ucieklak, Maciej Małecki et al.
Endokrynologia Polska
Diabetes Management and Research
article

Impact of the use of Extended™ Wear Infusion sets on metabolic, ultrasound, and psychological outcomes in adults with type 1 diabetes using the Medtronic MiniMed 780G: a pilot randomized controlled trial

Tomasz Klupa, Bartłomiej Matejko, Damian Ucieklak, Maciej Małecki, KATARZYNA M. CYRANKA, KAMILA SUSUL
article en

Abstract

INTRODUCTION: In people with type 1 diabetes (PwT1DM), insulin infusion sets (IIS) are often regarded as the most fragile componentof insulin pump therapy. Standard IISs should be replaced every 2-3 days to prevent site complications and hyperglycemia. The objectiveof this randomized controlled trial was to evaluate the impact of 7-day Extended™ Wear Infusion sets (EIS; Medtronic MiniMed,Northridge, CA, USA) on metabolic, ultrasound (USG), and psychological outcomes in PwT1DM treated with the MiniMed 780G system(MM780G, Medtronic MiniMed, Northridge, CA, USA). MATERIAL AND METHODS: Fifteen participants in both the intervention (EIS) and control groups (standard IIS) completed the 3-month study.One participant in the control group did not attend the follow-up USG examination; however, all other clinical, continuous glucose monitoring(CGM), and questionnaire data were available and included in the analyses. In the intervention group, the mean age was 36.1 ± 10.7years, diabetes duration 20.3 ± 7.6 years, body mass index (BMI) 24.9 ± 4.0 kg/m², and glycated hemoglobin A1c (HbA1c) 6.7 ± 0.5%. There were no significant baseline differences between groups in age, diabetes duration, CGM indices, or HbA1c. RESULTS: Across the study period, no statistically significant differences were observed between the control and intervention groups with respect to the number of lipohypertrophic lesions, the volume of the largest lesion, HbA1c, CGM indices or insulin requirements. Inboth groups (with no between-group differences), World Health Organization (WHO) 5 scores indicated improvements in psychologicalwell-being. Notably, 80% of participants reported that EIS were more comfortable than standard sets, and 73.3% stated that the newinfusion sets met their expectations. Two-thirds of participants found that the new infusion sets made life easier. CONCLUSIONS: These findings suggest that EIS are a safe and effective option for glycemic management in adults, without increasing lipohypertrophic lesions and with high patient acceptance.

Endokrynologia Polska
Jagiellonian University (PL), Szpital Uniwersytecki w Krakowie (PL)
Good health and well-being
Openalex Percentile: Top 11%
Diabetes Management and Research
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