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The efficacy of a non-invasive 1,060 nm diode laser for medial knee fat reduction

The efficacy of a non-invasive 1,060 nm diode laser for medial knee fat reduction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20220219002
Enrollment
19
Registered
2022-02-19
Start date
2018-08-16
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Medial knee fat 1,060 nm Diode laser fat reduction medial knee

Interventions

Female subjects complained of unwanted medial knee fat.
Treatment
unwanted medial knee fat

Sponsors

Faculty of Medicine Siriraj Hospital, Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All female subjects complained of unwanted medial knee fat. Presenting with body mass index (BMI) of 18.5 to 30 kg/m2.

Exclusion criteria

Exclusion criteria: The subjects with the following conditions were excluded from the study: pregnant or lactating women, previous history of liposuction and surgical procedures, previous treatment of botulinum injections and laser procedures, immunosuppressive disorders such as human immunodeficiency virus (HIV) infections and malignancies, those who are taking immunosuppressant drugs, previous history of herpes virus infection, underlying psychological conditions, history of hypertrophic scar or keloid formation, history of any skin infections and skin hypersensitivity or photosensitivity reaction.

Design outcomes

Primary

MeasureTime frame
mean kneecircumference baseline,1-month, 3-month, and 6-month follow-up visits after the treatment Direct measurement of knee circumference in cm

Secondary

MeasureTime frame
fat layer thickness baseline,1-month, 3-month, and 6-month follow-up visits after the treatment ultrasound,subject satisfaction 1-month, 3-month, and 6-month follow-up visits after the treatment All subjects answered the percentage improvement scale survey at every follow-up visit.,Side effects evaluation after treatment,1-month, 3-month, and 6-month follow-up visits after the treatment observe side effect

Countries

Thailand

Contacts

Public ContactRungsima Wanitphakdeedecha

Department of Dermatology Faculty of Medicine Siriraj Hospital

rungsima.wan@mahidol.ac.th6624194333

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026