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Therapeutic effect of Adipose-derived Stromal Vascular Fraction on Lateral Epicondylitis

Therapeutic effect of Adipose-derived Stromal Vascular Fraction on Lateral Epicondylitis (Tennis Elbow) disease, A randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221104056393N3
Enrollment
54
Registered
2024-01-11
Start date
2023-12-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Lateral epicondylitis. Lateral epicondylitis, unspecified elbow

Interventions

Intervention 1: About 100 mL of adipose tissue is taken under sterile condition through liposuction of the abdomen. The obtained fat will be emulsified by passing through 2.4 mm, 1.2 mm filters and fi

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: At least 4 months passed since onset of pain not responding to conservative therapy for 3 months A history of one unsuccessful corticosteroid or PRP injection in the past 3 months (at least 2 months have passed since the injection) The patient has the ability to understand the explanations and registers his oral and written desire in the informed consent form.

Exclusion criteria

Exclusion criteria: Any history of an injection in the elbow during the past 2 months History of cardiovascular disease such as previous myocardial infarction or heart failure Coagulopathies such as disrupted PT, PTT, INR Pregnancy or breastfeeding Drug users or alcoholics Elbow pain due to other musculoskeletal diseases such as rheumatoid arthritis, fibromyalgia, etc.

Design outcomes

Primary

MeasureTime frame
Elbow function. Timepoint: Before the intervention, 1, 3, 6 months after the intervention. Method of measurement: QuickDASH and MEPI questionnaire.

Secondary

MeasureTime frame
The patient's pain level. Timepoint: Before the intervention, 1, 3, 6 months after the intervention. Method of measurement: VAS questionnaire.;Radiological evaluation of the lesion in the form of CEO tendon lesion measurement. Timepoint: Before the intervention, 6 months after the intervention. Method of measurement: MRI examination by a radiologist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Robati

Shahid Beheshti University of Medical Sciences

rezarobati@sbmu.ac.ir+98 21 2274 1507

Outcome results

None listed

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