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Japanese

Oct. 18, 2024

Oct. 18, 2024

jRCTs041240108

A study of the efficacy and safety of sarcopenia therapy in Physically Inactive Patients with Type 2 Diabetes Mellitus (MIRAI-SARCOPENIA)

Efficacy of sarcopenia treatment in patients with type 2 diabetes mellitus

KOYAMA HIROYUKI

Nagoya City University Hospital

1, Kawasumi Mizuho-cho, Mizuho-ku, Nagoya, Aichi

+81-52-853-8211

hk0515@kuhp.kyoto-u.ac.jp

KOYAMA HIROYUKI

Nagoya City University Hospital

1, Kawasumi Mizuho-cho, Mizuho-ku, Nagoya, Aichi

+81-52-853-8211

hk0515@kuhp.kyoto-u.ac.jp

Recruiting

Oct. 18, 2024

20

Interventional

single arm study

open(masking not used)

uncontrolled control

single assignment

treatment purpose

1) Patients 65 years of age or older at the date of enrollment
2) Patients who meet the following sarcopenia diagnostic criteria (based on AWGS2019)
Grip strength: 28 kg or less in men and 18 kg or less in women
SMI (musculoskeletal index) measured by InBody: 7.0 kg/m2 or less in men and 5.4 kg/m2 or less in women.
3) Patients whose blood samples taken within 2 weeks prior to enrollment meet the following criteria
8.0% > HbA1c > 6.5
4) Patients who provide written consent for participation in the study

1) Patients with hyperglycemic emergencies, severe infections, major surgeries, or serious trauma within the past 6 months
2) Patients scheduled for surgery within the next 3 months
3) Patients who have already received prescriptions for EPA, EPA/DHA, or BCAA preparations
4) Patients with a history of allergy to EPA, EPA/DHA, or BCAA preparations in the past
5) Patients with bleeding (blood disease, active gastrointestinal ulcer, vitreous hemorrhage, etc.)
6) Patients with inborn errors of metabolism of branched-chain amino acids
7) Patients who are judged to be inappropriate as research subjects by the investigator(s), such as those who have difficulty in outpatient visits, those who are unlikely to be able to receive a certain intensity of rehabilitation.

65age old over
No limit

Both

Type 2 diabetes

Drug Therapy
(1) Lotriga Granular Capsules 2g once a day, immediately after meals
(2) Leebact granules: 3 times a day, after meals
Exercise Therapy
Twice a week, approximately 55 minutes of outpatient rehabilitation will be provided. The content of the exercise is as follows,
(1) Exercise using a chair (20 minutes)
(2) Upper and lower limb strength training using a strength training machine (30 minutes)
(3) Upper and lower limb stretching (5 minutes)

Change in skeletal muscle index

Amount of change in the following items before and after protocol treatment
Body weight, BMI
Blood pressure, pulse rate
GOT, GPT, TP, ALB, T-chol, TG, LDL-chol, HDL-chol, BUN, Cre, HbA1c, glycoalbumin, Cre/cystatin C ratio, ferritin, NT-ProBNP, lipoprotein(a), carnitine, TRACP-5b in blood tests, BAP, somatomedin C
TIR/TAR/TBR by FreeStyle Libre
SF-36 Questionnaire, Cognitive and Life Functioning Questionnaire (DASC-8), EAT-10 (swallowing screening tool), Questionnaire on Stages of Behavior Change (exercise items only)
Grip strength, chair stand test, TUG (Timed Up and Go) test
ABI, baPWV
T2 relaxation time of mediobasal hypothalamus, putamen, and amygdala in head MRI

Clinical Research Management Center, Nagoya City University Hospital
rinshou-kenkyu@med.nagoya-cu.ac.jp, Aichi

+81-52-853-8346

rinshou-kenkyu@med.nagoya-cu.ac.jp
Approval

Oct. 02, 2024

No

none