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Efficacy of autologous adipose tissue-derived mesenchymal stem cell therapy in Duchenne muscular dystrophic patients

Evaluation of safety and efficacy of autologous adipose-derived mesenchymal cells therapy in Duchenne muscular dystrophy patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150206020981N3
Enrollment
10
Registered
2022-06-07
Start date
2022-05-31
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Duchenne muscular dystrophy. Muscular dystrophy

Interventions

Intervention group: 100 to 150 cc of SVF product containing 20% mesenchymal cells, 60% progenitor cells and 20% other autologous cells in albumin medium will be injected intravenously through peripher

Sponsors

Research Deputy of Islamic Azad University, Tehran Medical Branch
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
7 Years to 30 Years

Inclusion criteria

Inclusion criteria: Genetic evidence of Duchenne disease as a cause of myopathy The patient's ability to walk is not completely lost and the use of assistive devices such as canes and walkers is not permanent. The patient's muscle strength is decreasing Willingness and satisfaction to participate in the study by the patient's legal guardian in decision making and willingness to participate regularly in follow-up courses

Exclusion criteria

Exclusion criteria: Advanced motor impairment leading to permanent use of crutches, walkers and wheelchairs A history of known malignancy History of associated genetic and non-genetic degenerative diseases Having blood and internal diseases that increase the risk of liposuction and anesthesia required A history of any other acute or chronic illness that, at the discretion of the clinician responsible for implementing the plan, prevents the patient from entering the study. Insufficient volume of subcutaneous fat or the presence of concomitant injuries in the abdomen in the initial examination that make it difficult to obtain adipose tissue to prepare SVF.

Design outcomes

Primary

MeasureTime frame
Respiratory Function. Timepoint: 1, 3, 6, 9 and 12 month after injection. Method of measurement: Spirometery.;Muscular Force. Timepoint: First every 14 days to 1 month, then Every 1 month to 1 year. Method of measurement: Physical Exam.;Cardiac Function. Timepoint: 1, 3, 6, 9 and 12 month after injection. Method of measurement: Echocardiography.

Secondary

MeasureTime frame
Muscular Enzymes. Timepoint: 1, 3, 6, 9 and 12 month after injection. Method of measurement: Lab Data.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKhadijeh Hajinaghi Tehrani

Bu-ali Hospital

Khtehrani@iautmu.ac.ir+98 21 3334 8035

Outcome results

None listed

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