Verification of safety and effectiveness in the treatment of rotator cuff tear of stromal vascular fractions

Prospective study for the safety and effect of autogenous adipose tissue derived stromal vascular fraction in repair of large-to-massive rotator cuff tear

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009542

Enrollment

Registered

2024-06-17

Start date

2024-06-03

Completion date

Unknown

Last updated

2024-06-24

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

Conditions

None listed

Interventions

Biological/Vaccine, Stem Cell, Others(stromal vascular fraction) : A portion of the abdominal fat tissue (60~120cc) is aspirated to obtain a stromal vascular fraction (4.2x10^7 ~ 6.0x10^7) and applied

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Men and women between 20 and 80 years of age

Exclusion criteria

Exclusion criteria: 1. Cases where complete suturing is impossible 2. History of trauma such as fracture in the relevant shoulder joint or history of previous surgery 3. When accompanied by rheumatoid arthritis or degenerative osteoarthritis 4. Patients with neurological disorders affecting the shoulder joint 5. Those who have confirmed pregnancy or are breastfeeding 6. Patients who have previously had abdominal liposuction or any type of ascites surgery 7. Patients who do not understand the questions used for patient evaluation or have communication problems 8. Patients who do not want to participate in the study or who find it difficult to visit the hospital according to the follow-up schedule 9. Other people deemed unsuitable by the research director

Design outcomes

Primary

Measure	Time frame
recurrence of tears	—

Secondary

Measure	Time frame
adverse effect	—

Countries

Korea, Republic of

Contacts

Public ContactChoi Jaehee

Asan Medical Center

Outcome results