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Effect of Silkworms (Bombyx Mori L.) Pupae Extracts on Musculoskeletal Biomarkers in Adults

Effect of Silkworms (Bombyx Mori L.) Pupae Extracts on Musculoskeletal Biomarkers in Adults With With Relatively Low Muscle Mass: a Randomized, Double-blinded, Placebo-controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04994054
Enrollment
54
Registered
2021-08-06
Start date
2021-07-05
Completion date
2022-02-28
Last updated
2023-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Brief summary

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of silkworms (Bombyx mori L.) pupae extracts on muscle strength, muscle mass, and muscle function in adults with relative sarcopenia for 12 weeks.

Detailed description

A previous study has indicated that silkworms (Bombyx mori L.) pupae extracts may increase muscle mass and strength. Therefore, the investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of silkworms (Bombyx mori L.) pupae extracts on muscle strength, muscle mass, and muscle function in adults with relative sarcopenia; the safety of the compound are also evaluated. The Investigators examine the peak torque/body weight at 60°/s knee extension, handgrip strength, skeletal muscle mass, physical performance, and metabolic parameters at baseline, as well as after 12 weeks of intervention. Fifty four adults were administered either 2,400 mg of silkworms (Bombyx mori L.) pupae extracts or a placebo each day for 12 weeks.

Interventions

DIETARY_SUPPLEMENTsilkworms (Bombyx mori L.) pupae extracts group

silkworms (Bombyx mori L.) pupae extracts 2,400 mg/day for 12 weeks

DIETARY_SUPPLEMENTPlacebo group

Placebo 2,400 mg/day for 12 weeks

Sponsors

Pusan National University Yangsan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* \<110% of the standard lean body mass as measured using the body composition analyzer * Body mass index (BMI) ranging from 18.5 to 30.0 kg/m2

Exclusion criteria

* Vegetarian * History of any central bone fracture within 1 year * History of cancer or serious cerebro-cardiovascular diseases within 6 months * Abnormal liver or renal function (more than twice the normal upper limit of the research institute) * Uncontrolled diabetes mellitus (\>160 mg/dL of fasting blood sugar) * Uncontrolled hypertension (\>160/100 mmHg) * Uncontrolled thyroid diseases. * History of medication for psychiatric diseases such as severe affective disorder, schizophrenia, and substance use. * Alcohol abuser * Allergic reaction to constituent foods * Severe gastrointestinal symptoms such as heartburn and indigestion * Those who are pregnant, lactating, or planning to become pregnant during the clinical trial * Those who have participated in other drug clinical trials within the last 3months

Design outcomes

Primary

MeasureTime frameDescription
the peak torque at 60°/s knee extension (/kg)12 weeksconducted on the Biodex System 3 Pro isokinetic dynamometer (Biodex, Inc.)

Secondary

MeasureTime frameDescription
skeletal Muscle Mass Index/(height x height)12 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
concentration of creatinine kinase (IU/L)12 weekscreatinine kinase (IU/L) measured at baseline and after 12 weeks
concentration of creatine (mg/dL)12 weekscreatine (mg/dL) measured at baseline and after 12 weeks
appendicular skeletal mass/(height x height)12 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
EuroQol five dimensional five levels12 weeksan index of life quality, minimum, maximum values (-0.171, 1), higher scores mean a better outcome, which will be measured at baseline and after 12 weeks
appendicular skeletal mass/weight x 10012 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
body weight (kg)12 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
skeletal musle mass (kg)12 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
total fat percent (%)12 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
truncal fat percent (%)12 weeksusing dual-energy X-ray absorptiometry measured at baseline and after 12 weeks
handgrip strength (kg), right and left12 weeksusing a hydraulic hand dynamometer (Jamar)

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026