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A Clinical Study on the Effect of Pei Tu Sheng Ji Electroacupuncture in Treating Sarcopenia by Regulating C-terminal Agrin Fragment

A Clinical Study on the Effect of Peitu Shengji Electroacupuncture in Treating Sarcopenia by Regulating C-terminal Agrin Fragment

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122080
Enrollment
Unknown
Registered
2026-04-08
Start date
2026-04-13
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Sarcopenia

Interventions

Trial Group:Peitu Shengji electroacupuncture (acupoints: Jianyu, Zhongli, Wuli of Hand Yangming
Zusanli, Biguang, Xijuyu of Foot Yangming. Needle size: 50mm*0.2mm, inserted straight to obtain Qi, connected to electroacupuncture device with intermittent wave, frequency 4 Hz, current intensity adj
3 times per week on Mondays, Wednesdays, Fridays, each session lasting 20 minutes) combined with basic treatment (exercise training + nutritional support + health education)
Control Group:Sham electroacupuncture at non-acupoints (2cm beside the acupoints used in the trial group, needle size: 25mm*0.2mm, shallow insertion 1-3mm, no manipulation to avoid obtaining Qi
connected to electroacupuncture device with intermittent wave, frequency 4 Hz, current intensity adjusted for patient comfort

Sponsors

Sichuan Academy of Medical Sciences · Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for sarcopenia; patients must simultaneously meet the criteria for low muscle strength and low muscle mass (referencing the Asian Working Group for Sarcopenia (AWGS) 2025 Consensus Update): (1) Low muscle strength (handgrip strength): Aged 50~64 (Male = 65 (Male = 65 (Male < 7.0 kg/m^2, Female < 5.4 kg/m^2). 2. Absence of other cachexia or diseases causing sarcopenia. 3. No gender restriction. 4. Have not received regular treatment for sarcopenia within the past year. 5. Capable of understanding the trial process, rights, and obligations, and willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Cognitive dysfunction affecting the understanding of the trial process, rights, and obligations. 2. Severe mental illness, dementia, or other conditions preventing cooperation with the trial. 3. Comorbidities such as disability or severe bone/joint diseases that would affect the progress and results of the trial. 4. Abnormal liver or kidney function (Cr > 82 µmol/L, AST > 35 U/L), as the trial requires observation of serum markers related to liver and kidney function. 5. Currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
6-meter gait speed;

Secondary

MeasureTime frame
Appendicular Skeletal Muscle Mass (ASM);Calf circumference;Handgrip strength; SPPB functional scale;5-time chair stand test time;C-terminal agrin fragment (CAF);Irisin;Cr/CysC;

Countries

China

Contacts

Public ContactZhang Yun

Sichuan Academy of Medical Sciences · Sichuan Provincial People's Hospital

cry261979@126.com+86 189 8183 8369

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026