Skip to content

Clinical safety evaluation and preliminary efficacy study of subcutaneous myografts transplantation

Clinical safety evaluation and preliminary efficacy study of subcutaneous myografts transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118734
Enrollment
Unknown
Registered
2026-02-10
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Muscle damage and degeneration

Interventions

Myografts transplantation group:Myografts are taken from a healthy area and transplanted to the subcutaneous site of injury and degeneration.

Sponsors

National Clinical Research Center for Orthopedics, Sports Medicine & Rehabilitation-Binhai Yangshi Orthopedic Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 65 years, regardless of gender. 2. The patient's underlying disease is stable and not in an acute exacerbation phase. 3. The patient has muscle injury and degeneration requiring autologous muscle flap transplantation. 4. Written informed consent has been obtained from the patient, immediate family members, or legal guardians, agreeing to undergo the transplantation procedure.

Exclusion criteria

Exclusion criteria: 1. History of malignant tumor; 2. Coagulation dysfunction or use of anticoagulant drugs; 3. Active infection or immunodeficiency; 4. Severe renal or cardiac dysfunction (eGFR 3 times the upper limit of normal); 6. Local severe skin lesions, or previous history of injection site allergic reactions; 7. Use of muscle growth regulatory drugs (such as testosterone, growth hormone) within the past 6 months. 8. Long-term use of hormones or immunosuppressants, including the application of anti-rejection drugs after organ transplantation. 9. Other exclusion factors: participation in other interventional clinical trials (excluding observational studies). 10. The investigator believes that there are other medical or ethical factors that make the subject ineligible for inclusion.

Design outcomes

Primary

MeasureTime frame
Basic vital sign monitoring;Local adverse reactions;Evaluation of graft survival;Inflammation and immune status;Liver enzyme indicators;Muscle mass;Muscle thickness;Detection of muscle secreted muscle factors;

Secondary

MeasureTime frame
Bone density assessment;Blood lipid profile test;Evaluation of Blood Glucose and Insulin Resistance;Energy consumption monitoring;Fat content assessment;

Countries

China

Contacts

Public ContactPengbin Yin

National Clinical Research Center for Orthopedics, Sports Medicine & Rehabilitation-Binhai Yangshi Orthopedic Hospital

yinpengbin@gmail.com+86 150 1049 7628

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026