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Clinical study on the effect of three kinds of unsaturated fatty acids on skeletal muscle function and gut microbiome in patients with sarcopenia

Clinical study on the effect of three kinds of unsaturated fatty acids on skeletal muscle function and gut microbiome in patients with sarcopenia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043620
Enrollment
Unknown
Registered
2021-02-23
Start date
2021-09-01
Completion date
Unknown
Last updated
2021-06-22

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

Conditions

Sarcopenia

Interventions

Omega-6 intervention group:Supplement 33g omega-6 daily
Omega-9 intervention group:Supplement 33g omega-9 daily
Omega-6 +omega-3 intervention group:Supplement 3g omega-3 capsules and 30g omega-6 daily
Omega-9 +omega-3 intervention group:Supplement 3g omega-3 capsules and 30g omega-9 daily
omega-3 intervention group:Supplement 3g omega-3 capsules and 30g omega-3 daily

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age 65-85 years old; 2. Patients diagnosed with sarcopenia according to the latest Asian diagnostic criteria for sarcopenia; 3. Patients with no obvious abnormalities in blood lipids (TG: 1.70~2.25mmol/L); 4. Patients who are expected to not leave their place of residence within six months and have good compliance; 5. Patients who are willing to participate in this trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from cardiovascular diseases, liver diseases, lung diseases, kidney diseases, severe hyperlipidemia, infectious diseases, etc.; 2. Patients who are allergic to deep-sea fish, olives, soybeans and their products; 3. Patients who have a history of using antibiotics within 2 weeks before enrollment, or who are taking drugs that affect the study (such as hormone drugs, steroid drugs, and weight loss drugs, etc.); 4. Patients with severe cognitive impairment or the history of psychotropic drug abuse; 5. Patients who are participating in other nutrition or gut microbiome intervention projects; 6. Patients who do not agree to participate in the study, cannot complete the trial, or expect to be unable to obtain follow-up data.

Design outcomes

Primary

MeasureTime frame
Physical function;The bundance and diversity of fecal gut microbiome;

Secondary

MeasureTime frame
erumOmega-3 Concentration;Serum Omega-6 Concentration;Serum Omega-9 Concentration;Grip strength (Muscle strength,Biceps strength, knee extensor strength, hip flexor strength );Walking speed;fecal lipid metabolisim;blood lipids;IL-6;TNF-a;Serum albumin;

Countries

China

Contacts

Public ContactYu Zhen

Shanghai Tenth People's Hospital

yuzhen0577@163.com+86 18917687560

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026