The Evaluation of Laser Lancing Devices in Adult Type 2 Diabetes Patients

Korea University

Status: Unknown

Conditions: Type 2 Diabetes

Treatments: Device: laser lancing device or lancet for blood glucose level measurement

Study type: Interventional

Funder types: Other

Identifiers

NCT05251506

K2021-1520-002

Details and patient eligibility

About

Self monitoring of blood glucose level is crucial in diabetes management, but currently available methods, lancet, have shown low compliance of self monitoring of blood glucose because of pain, keratinization of finger tip, secondary infection. The purpose of this study is evaluating laser lancing device which cause much less pain than lancet to increase compliance of blood sugar checking, and to establish self monitoring system for patients of chronic diseases.

The investigators recruit total of 80 type 2 diabetes patients who visit Korea University Medical center Guro and Ansan hospital. HbA1c level of subject is more than 6.5% and less than 8.5%, and their age is above 20 years and under 80 years. Subjects are randomly distributed in group A or B. Group A subjects use laser device to check blood glucose for 2 months, then take a month for wash out period. After wash out period, participants use lancet for following 2 months. Group B perform the process vice versa. The investigators evaluate the number of blood glucose measurement, HbA1c, diabetes distress scale, average pain score, average satisfaction score from each group.

Full description

Self monitoring of blood glucose level is crucial in diabetes management, so it is important to increase compliance of blood glucose checking. Lancet which is currently available methods have shown low compliance of self monitoring of blood glucose, since it causes pain, keratinization of finger tip, secondary infection. The purpose of this study is evaluating laser lancing device which cause much less pain than lancet to increase compliance of blood sugar checking, and to establish self monitoring system for patients of chronic diseases.

The investigators recruit total of 80 subjects who visit Korea University Medical center Guro and Ansan hospital. Study subject are type 2 diabetes whose glycated hemoglobin level is more than 6.5% and less than 8.5%, and whose age is more than 20 years and under 80 years. Subjects are randomly distributed in group A or B. Group A subjects use laser device to check blood glucose for 2 months, then take a month for wash out period. After wash out period, participants use lancet for following 2 months. Group B subjects use lancet first, then have a month for wash out period, after then, switch to laser device afterwards. During washout period, participants use usual glucose checking method which subjects had used. The investigators evaluate the number of blood glucose measurement, glycated hemoglobin, diabetes distress scale, average pain score, average satisfaction score from each group. Also the investigators compare blood glucose, liver function test, lipid level between values from one hand measured by lancet, and values from the other hand measured by laser lancing device.

Enrollment: 80 estimated patients

Sex: All

Ages: 20 to 79 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Type 2 diabetes patients who visit Korea University medical center, Guro hospital, Ansan hospital
• Patients with Hba1c more than 6.5% and less than 8.5%
• Adults who are able to measure blood glucose level by themselves
• Adults who are able to lance their same finger from both hands
• Adults who comprehend risk of participating in the clinical research, who are able to communicate each other, who are able to follow rules of clinical research
• Subjects who decide to participate in the clinical research voluntarily and sign in the consent format after being informed purposes, methods, expectations of the clinical research

Exclusion criteria

• Subject whose age is younger than 19 or older than 80
• students of research institutes
• Pregnant and lactating women
• Subjects who are not able to make decision
• Subjects who are in emergency or being hospitalized
• Subjects who cannot lance sane finger from both hands
• Subjects who are infected by HIV in hospital records
• Subjects who have thrombocytopenia, coagulation disorder or haemophilia
• Subjects who are incompatible for clinical research as researcher evaluated

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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80 participants in 2 patient groups

laser lancing device (LMT-1000) first user

Experimental group

Description:

Subjects measure blood glucose using laser lancing device (LMT-1000) for first 2 months, then take a month for wash out period, after that do using lancet for following 2 months.

Treatment:

Device: laser lancing device or lancet for blood glucose level measurement

lancet first user

Active Comparator group

Description:

Subjects measure blood glucose using lancet for first 2 months, , then take a month for wash out period, after that do using laser lancing device (LMT-1000) for following 2 months.

Treatment:

Device: laser lancing device or lancet for blood glucose level measurement